EP3141570B1 - Résine produite par polycondensation, et composition de résine - Google Patents

Résine produite par polycondensation, et composition de résine Download PDF

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Publication number
EP3141570B1
EP3141570B1 EP15789371.0A EP15789371A EP3141570B1 EP 3141570 B1 EP3141570 B1 EP 3141570B1 EP 15789371 A EP15789371 A EP 15789371A EP 3141570 B1 EP3141570 B1 EP 3141570B1
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Prior art keywords
structural unit
group
general formula
resin
compound represented
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German (de)
English (en)
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EP3141570A4 (fr
EP3141570A1 (fr
Inventor
Noriyuki Kato
Hirohito Ishizuka
Munenori Shiratake
Kentaro Ishihara
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Mitsubishi Gas Chemical Co Inc
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Mitsubishi Gas Chemical Co Inc
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Priority to EP18201503.2A priority Critical patent/EP3483197A1/fr
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Publication of EP3141570A4 publication Critical patent/EP3141570A4/fr
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
    • C08G64/04—Aromatic polycarbonates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/16—Dicarboxylic acids and dihydroxy compounds
    • C08G63/18—Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
    • C08G63/19—Hydroxy compounds containing aromatic rings
    • C08G63/193—Hydroxy compounds containing aromatic rings containing two or more aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
    • C08G64/16—Aliphatic-aromatic or araliphatic polycarbonates
    • C08G64/1608—Aliphatic-aromatic or araliphatic polycarbonates saturated
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/16—Dicarboxylic acids and dihydroxy compounds
    • C08G63/18—Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
    • C08G63/19—Hydroxy compounds containing aromatic rings
    • C08G63/193—Hydroxy compounds containing aromatic rings containing two or more aromatic rings
    • C08G63/197—Hydroxy compounds containing aromatic rings containing two or more aromatic rings containing condensed aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/64—Polyesters containing both carboxylic ester groups and carbonate groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/66—Polyesters containing oxygen in the form of ether groups
    • C08G63/668—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/672—Dicarboxylic acids and dihydroxy compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
    • C08G64/04—Aromatic polycarbonates
    • C08G64/06—Aromatic polycarbonates not containing aliphatic unsaturation
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/005—Stabilisers against oxidation, heat, light, ozone
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/02—Halogenated hydrocarbons
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/04—Oxygen-containing compounds
    • C08K5/10—Esters; Ether-esters
    • C08K5/101—Esters; Ether-esters of monocarboxylic acids
    • C08K5/103—Esters; Ether-esters of monocarboxylic acids with polyalcohols
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/04—Oxygen-containing compounds
    • C08K5/13—Phenols; Phenolates
    • C08K5/134—Phenols containing ester groups
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
    • G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
    • G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
    • G02B1/041—Lenses
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/20—Light-sensitive devices
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K10/00—Organic devices specially adapted for rectifying, amplifying, oscillating or switching; Organic capacitors or resistors having potential barriers
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00—Organic light-emitting devices
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/90—Applications
    • C08G2261/91—Photovoltaic applications
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00—Energy generation through renewable energy sources
    • Y02E10/50—Photovoltaic [PV] energy
    • Y02E10/549—Organic PV cells

Definitions

  • the present invention relates to a resin produced by polycondensation, which comprises a structural unit having a specific binaphthyl skeleton and a structural unit having a specific fluorene structure, and a resin composition.
  • optical glasses As a material of optical elements to be used in optical systems of various cameras such as cameras, film integrated type cameras and video cameras, an optical glass or an optical transparent resin is used.
  • Optical glasses are excellent in heat resistance, transparency, size stability, chemical resistance, etc., and there are various optical glasses with different refractive indexes or Abbe numbers.
  • optical glasses have problems of high material costs, bad molding processability and low productivity. In particular, significantly advanced techniques and high costs are required for processing for obtaining an aspherical lens to be used for aberration correction, and this is a major obstacle from a practical viewpoint.
  • optical lenses made of optical transparent resins can be mass-produced by injection molding, and in addition, an aspherical lens can be easily produced therefrom.
  • optical lenses are currently used as camera lenses.
  • optical transparent resins include a polycarbonate made of bisphenol A, a polymethyl methacrylate and an amorphous polyolefin.
  • aberration is corrected by combining a plurality of concave lenses and convex lenses.
  • chromatic aberration is synthetically corrected by combining convex lenses having chromatic aberration with concave lenses having chromatic aberration whose sign is opposite to that of the chromatic aberration of the convex lenses.
  • the concave lenses are required to have high dispersion (i.e., a low Abbe number).
  • the polycarbonate made of bisphenol A has a refractive index of about 1.59 and an Abbe number of about 32
  • the polymethyl methacrylate has a refractive index of about 1.49 and an Abbe number of about 58
  • the amorphous polyolefin has a refractive index of about 1.54 and an Abbe number of about 56.
  • the polycarbonate can be used as concave lenses for aberration correction, but when the Abbe number is 32, it cannot be said that sufficiently high dispersion is obtained thereby. For this reason, a novel material which can be used as concave lenses for aberration correction has been desired.
  • Patent Document 1 discloses a polyester resin composition obtained by copolymerization of a fluorene-based dihydroxy compound having a refractive index of about 1.66 and an Abbe number of about 20.
  • the polycarbonate resin made of bisphenol A is widely used for optical lenses, but applications of the polycarbonate resin are limited because of high birefringence thereof as a drawback.
  • a resin material having high imaging performance and low birefringence has been desired.
  • Examples of methods for realizing low birefringence of resin materials include a technique of canceling positive birefringence of a composition with negative birefringence of another composition (Patent Document 5).
  • the sign (positive or negative) of birefringence is determined by the difference between the polarizability of the polymer main chain direction and the polarizability of the polymer side chain direction.
  • a polycarbonate resin made of bisphenol having a fluorene structure in which the polarizability of the polymer side chain direction is larger has negative birefringence.
  • the component ratio of materials whose birefringence signs are opposite to each other is very important.
  • Patent Document 6 describes that use of a dicarboxylic acid having a fluorene structure as a raw material in a polyester resin is effective for reduction of birefringence.
  • carboxylic acid is a type of a compound having a hydroxyl group (Non-Patent Document 1).
  • Patent Documents 2, 3 and 4 do not disclose any resin having a structural unit derived from a compound represented by general formula (1).
  • Patent Document 4 describes a polymer comprising a structural unit represented by general formula (A), but it is not a polymer comprising a structural unit having a fluorene structure. Further, the patent document does not disclose whether the sign of birefringence of the polymer comprising a structural unit represented by general formula (A) is positive or negative.
  • X represents a C 1-10 alkylene group.
  • A represents a C 2-4 alkylene group.
  • the naphthalene ring may be substituted with a substituent, and substituted substituents may be subjected to ring condensation, m and 1 respectively represent an integer of 0 ⁇ m ⁇ 50 and an integer of 0 ⁇ 1 ⁇ 50.
  • Non-Patent Document 1 Renji Okazaki, "Iwanami Lecture Series, Introduction to Modern Chemistry ⁇ 9> Characteristics and Molecular Transform of Organic Compounds", Iwanami Shoten, 2004, page 96 (in Japanese )
  • the purpose of the present invention is to provide a resin having excellent optical characteristics such as a high refractive index and a low Abbe number in view of the above-described problems.
  • a resin obtained by using a specific monomer particularly provides optically superior performance, for example, a high refractive index and a low Abbe number.
  • the present invention is, for example, as follows:
  • the resin of the embodiment of the present invention is a resin produced by polycondensation using at least a compound represented by general formula (1) and a compound represented by general formula (2) as raw materials.
  • the resin produced by polycondensation is polyester or polyester carbonate.
  • the structural unit derived from the compound represented by general formula (1) contributes to a high refractive index, and in addition, contributes to reduction of the Abbe number more than the structural unit derived from the compound represented by general formula (2).
  • the structural unit derived from the compound represented by general formula (2) contributes to a high refractive index and a low Abbe number, and in addition, has effects of reducing a birefringence value derived from the compound represented by general formula (1) and reducing optical distortion of an optical molded body.
  • Optical characteristics such as the refractive index, Abbe number and birefringence value are significantly affected by chemical structures of structural units, and the influence related to the matter as to whether a chemical bond between structural units is an ester bond or carbonate bond is relatively small.
  • the functional group which contributes to polycondensation is an alcoholic hydroxyl group.
  • a typical example of the functional group which contributes to polycondensation is a hydroxyl group, and examples thereof include an alcoholic hydroxyl group, a phenolic hydroxyl group and a carboxylic hydroxyl group.
  • the resin of the embodiment has a structural unit derived from a dihydroxy compound (excluding dicarboxylic acid) and a structural unit derived from a dicarboxylic acid, but it does not mean that raw materials of the resin are limited to the dihydroxy compound and the dicarboxylic acid.
  • raw materials of the resin are limited to the dihydroxy compound and the dicarboxylic acid.
  • an ester, an acid anhydride and an acid halide of the dicarboxylic acid may also be used as raw materials.
  • a component derived from the dihydroxy compound in the resin is sometimes referred to as a "dihydroxy component” or “dihydroxy structural unit”
  • a component derived from the dicarboxylic acid is sometimes referred to as a “dicarboxylic acid component” or “dicarboxylic acid structural unit”.
  • carboxylic acid is a type of hydroxy compound
  • dicarboxylic acid is a type of dihydroxy compound.
  • a resin composition obtained by mixing a resin obtained by polycondensation of at least the compound represented by general formula (1) and a resin obtained by polycondensation of at least the compound represented by general formula (2) are described. Accordingly, the resin composition contains the structural unit derived from the compound represented by general formula (1) and the structural unit derived from the compound represented by general formula (2).
  • Optical characteristics such as the refractive index, Abbe number and birefringence value are significantly affected by structures of these structural units, and the influence related to the matter as to whether the structural units exist in one molecule as in the case of copolymers or exist in a plurality of molecules as in the case of mixtures is relatively small.
  • Examples of the dihydroxy compound represented by general formula (1) include 2,2'-bis(hydroxymethoxy)-1,1'-binaphthalene, 2,2'-bis(2-hydroxyethoxy)-1,1'-binaphthalene, 2,2'-bis(3-hydroxypropyloxy)-1,1'-binaphthalene and 2,2'-bis(4-hydroxybutoxy)-1,1'-binaphthalene.
  • 2,2'-bis(2-hydroxyethoxy)-1,1'-binaphthalene is preferably used.
  • R 1 and R 2 each independently represent a hydrogen atom, a C 1-20 alkyl group, a C 1-20 alkoxyl group, a C 5-20 cycloalkyl group, a C 5-20 cycloalkoxyl group, a C 6-20 aryl group or a C 6-20 aryloxy group and R represents a hydrogen atom or a C 1-20 hydroxyalkyl group.
  • a compound having a fluorene structure represented by general formula (2a) or (2b) is preferably used. It is sufficient when at least one of such compounds is used, and two or more of them may be used in combination.
  • R 1 and R 2 each independently represent a hydrogen atom, a C 1-20 alkyl group, a C 1-20 alkoxyl group, a C 5-20 cycloalkyl group, a C 5-20 cycloalkoxyl group, a C 6-20 aryl group or a C 6-20 aryloxy group.
  • R 1 and R 2 preferred is a hydrogen atom, a C 1-12 alkyl group or a C 6-12 aryl group; more preferred is a hydrogen atom, a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a cycloheptyl group, a cyclopropyl group or a phenyl group; and particularly preferred is a hydrogen atom, a methyl group or a phenyl group.
  • Examples of the dihydroxy compound represented by formula (2a) include 9,9-bis(4-(2-hydroxyethoxy)phenyl)fluorene, 9,9-bis(4-(2-hydroxyethoxy)-3-methylphenyl)fluorene, 9,9-bis(4-(2-hydroxyethoxy)-3,5-dimethylphenyl)fluorene, 9,9-bis(4-(2-hydroxyethoxy)-3-tert-butylphenyl)fluorene, 9,9-bis(4-(2-hydroxyethoxy)-3-isopropylphenyl)fluorene, 9,9-bis(4-(2-hydroxyethoxy)-3-cyclohexylphenyl)fluorene and 9,9-bis(4-(2-hydroxyethoxy)-3-phenylphenyl)fluorene.
  • R 1 and R 2 each independently represent a hydrogen atom, a C 1-20 alkyl group, a C 1-20 alkoxyl group, a C 5-20 cycloalkyl group, a C 5-20 cycloalkoxyl group, a C 6-20 aryl group or a C 6-20 aryloxy group.
  • R 1 and R 2 preferred is a hydrogen atom, a C 1-12 alkyl group or a C 6-12 aryl group; more preferred is a hydrogen atom, a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a cycloheptyl group, a cyclopropyl group or a phenyl group; and particularly preferred is a hydrogen atom or a methyl group.
  • Examples of the dihydroxy compound represented by formula (2b) include 9,9-bis(4-hydroxyphenyl)fluorene, 9,9-bis(4-hydroxy-3-methylphenyl)fluorene, 9,9-bis(4-hydroxy-3-ethylphenyl)fluorene, 9,9-bis(4-hydroxy-3-n-propylphenyl)fluorene, 9,9-bis(4-hydroxy-3-isopropylphenyl)fluorene, 9,9-bis(4-hydroxy-3-n-butylphenyl)fluorene, 9,9-bis(4-hydroxy-3-sec-butylphenyl)fluorene, 9,9-bis(4-hydroxy-3-tert-butylphenyl)fluorene, 9,9-bis(4-hydroxy-3-cyclohexylphenyl)fluorene, 9,9-bis(4-hydroxy-2-phenylphenyl)fluorene, 9,9-bis(4-hydroxy-3-phenyl
  • 9,9-bis(4-hydroxy-3-phenylphenyl)fluorene and 9,9-bis(4-hydroxy-3-methylphenyl)fluorene are preferred. These compounds may be used solely, or two or more of them may be used in combination.
  • the resin of the present invention is a polyester or a polyester carbonate.
  • these resins will be respectively described in detail.
  • the present invention relates to a resin composition comprising a polycarbonate resin as defined in the claims.
  • the polycarbonate resin used in the present invention is a polycarbonate resin having: a structural unit derived from a compound represented by general formula (1) (hereinafter sometimes referred to as “structural unit (A)”); and a structural unit derived from a compound represented by general formula (2) (excluding carboxylic acid) (hereinafter sometimes referred to as “structural unit (B)”).
  • structural unit (A) a structural unit derived from a compound represented by general formula (1)
  • structural unit (2) excluding carboxylic acid
  • a compound represented by general formula (2a) and a compound represented by general formula (2b) can be suitably used.
  • R 1 and R 2 are as defined with respect to formula (2) above.
  • R 1 and R 2 are as defined with respect to formula (2) above.
  • an aromatic dihydroxy compound and an aliphatic dihydroxy compound can be used in combination.
  • Polycarbonate resin comprising a structural unit derived from a compound represented by general formula (2a)
  • the polycarbonate resin preferably comprises a structural unit (A) derived from a compound represented by general formula (1) and a structural unit derived from a compound represented by general formula (2a) (hereinafter sometimes referred to as "structural unit (C)").
  • the ratio of the total of the carbonate unit induced from the structural unit (A) and the carbonate unit induced from the structural unit (C) is preferably 50 mol% or more, more preferably 80 mol% or more, particularly preferably 90 mol% or more, and most preferably 100 mol% relative to all the carbonate units constituting the polycarbonate resin.
  • the polycarbonate resin may contain a structural unit other than the structural units (A) and (C).
  • the molar ratio between the structural unit (A) and the structural unit (C) (A/C) is preferably 20/80 to 99/1, more preferably 30/70 to 95/5, and particularly preferably 40/60 to 90/10.
  • the ratio of the carbonate unit induced from the structural unit (A) is preferably 1 to 99 mol% relative to all the carbonate units constituting the polycarbonate resin.
  • the ratio of the carbonate unit induced from the structural unit (A) is more preferably 30 to 90 mol%, and even more preferably 40 to 80 mol% relative to all the carbonate units constituting the polycarbonate resin.
  • the polystyrene equivalent weight-average molecular weight (Mw) of the polycarbonate resin is preferably 20000 to 200000.
  • the polystyrene equivalent weight-average molecular weight (Mw) is more preferably 25000 to 120000, even more preferably 25000 to 60000, and particularly preferably 40000 to 60000.
  • Mw is less than 20000
  • a molded body becomes fragile and therefore it is undesirable.
  • Mw is more than 200000
  • the melt viscosity increases, resulting in difficulty in taking out a resin from a mold at the time of molding, and in addition, the flowability is reduced, resulting in difficulty in injection molding in a molten state, and therefore it is undesirable.
  • the polycarbonate resin may have a structure of either a random copolymer, block copolymer or alternating copolymer.
  • the refractive index (nD) of the polycarbonate resin at 23°C at a wavelength of 589 nm is preferably 1.640 to 1.680, more preferably 1.645 to 1.675, and even more preferably 1.650 to 1.670.
  • the above-described polycarbonate resin has a high refractive index (nD) and is suitable as an optical lens material.
  • the refractive index can be measured by the method of JIS-K-7142 using a film having a thickness of 0.1 mm and an Abbe's refractometer.
  • the Abbe number (v) of the polycarbonate resin is preferably 24 or less, more preferably 23 or less, and even more preferably 22 or less.
  • the glass transition temperature (Tg) is preferably 95 to 180°C, more preferably 110 to 170°C, even more preferably 115 to 160°C, and particularly preferably 125 to 145°C.
  • Tg is lower than 95°C, the operating temperature range is narrowed, and therefore it is undesirable.
  • Tg is higher than 180°C, the melting temperature of the resin increases, decomposition and coloring of the resin tend to be easily caused, and therefore it is undesirable.
  • the glass transition temperature of the resin is too high, in the case of using a widely-used mold temperature controller, the difference between the mold temperature and the glass transition temperature of the resin increases. For this reason, it is difficult to use a resin having a too high glass transition temperature for applications which require exact surface accuracy of products, and therefore it is undesirable.
  • the 5% weight reduction temperature (Td) of the polycarbonate resin measured at a temperature raising rate of 10°C/min is preferably 350°C or higher.
  • the resin is thermally decomposed significantly at the time of molding and it is difficult to obtain a good molded body, and therefore it is undesirable.
  • the orientation birefringence ( ⁇ n) that is a scale of the amount of birefringence is preferably 1.0 ⁇ 10 -3 or less, more preferably 0.8 ⁇ 10 -3 or less, even more preferably 0.3 ⁇ 10 -3 or less, and particularly preferably 0.2 ⁇ 10 -3 or less.
  • ⁇ n Re / d
  • ⁇ n n / / ⁇ n ⁇
  • the phenol content in the polycarbonate resin is preferably 0.1 to 3000 ppm, more preferably 0.1 to 2000 ppm, and particularly preferably 1 to 1000 ppm, 1 to 800 ppm, 1 to 500 ppm or 1 to 300 ppm.
  • the carbonic acid diester content in the polycarbonate resin is preferably 0.1 to 1000 ppm, more preferably 0.1 to 500 ppm, and particularly preferably 1 to 100 ppm.
  • the content of phenol or carbonic acid diester When the content of phenol or carbonic acid diester is more than the above-described ranges, it may cause problems such as reduction in the strength of a resin molded body obtained and generation of odor. Meanwhile, when the content of phenol or carbonic acid diester is less than the above-described ranges, it may cause reduction in the plasticity of a resin at the time of melting.
  • the total light transmittance of an optical molded body obtained by using the polycarbonate resin is preferably 85% or more, and more preferably 88% or more, and is comparable to those of a bisphenol A-type polycarbonate resin, etc.
  • an antioxidant e.g., an antioxidant, a mold release agent, an ultraviolet absorber, a flowability improving agent, a crystal nucleating agent, a toughening agent, a dye, an antistatic agent, or an antimicrobial agent may be added.
  • the polycarbonate resin having a structural unit derived from a compound represented by general formula (2a) can be produced by the melt polycondensation method using a compound represented by general formula (1), a compound represented by general formula (2a) and a carbonate precursor such as a carbonic acid diester in the presence or absence of a basic compound catalyst or a transesterification catalyst or a mixed catalyst made of both of them.
  • Examples of the carbonic acid diester to be used in the reaction include diphenyl carbonate, ditolyl carbonate, bis(chlorophenyl) carbonate, m-cresyl carbonate, dimethyl carbonate, diethyl carbonate, dibutyl carbonate and dicyclohexyl carbonate. Among them, diphenyl carbonate is particularly preferred.
  • the carbonic acid diester is used at a ratio of preferably 0.97 to 1.20 mol, and more preferably 0.98 to 1.10 mol relative to 1 mol of the total of the dihydroxy compounds. When the amount of the carbonic acid diester is not within these ranges, for example, problems that a resin does not have a desired molecular weight, and that an unreacted raw material remains in a resin, resulting in reduction in optical characteristics may be caused.
  • Examples of the basic compound catalyst particularly include an alkali metal compound, an alkaline earth metal compound and a nitrogen-containing compound.
  • alkali metal compound examples include an organic salt, inorganic salt, oxide, hydroxide, hydride or alkoxide of an alkali metal, etc.
  • Specific examples thereof include sodium hydroxide, potassium hydroxide, cesium hydroxide, lithium hydroxide, sodium hydrogen carbonate, sodium carbonate, potassium carbonate, cesium carbonate, lithium carbonate, sodium acetate, potassium acetate, cesium acetate, lithium acetate, sodium stearate, potassium stearate, cesium stearate, lithium stearate, sodium borohydride, sodium tetraphenylborate, sodium benzoate, potassium benzoate, cesium benzoate, lithium benzoate, disodium hydrogen phosphate, dipotassium hydrogen phosphate, dilithium hydrogen phosphate, disodium phenyl phosphate, a disodium salt, dipotassium salt, dicesium salt or dilithium salt of bisphenol A, and a sodium salt, potassium salt, cesium salt or lithium salt of phenol.
  • alkaline earth metal compound examples include an organic salt, inorganic salt, oxide, hydroxide, hydride or alkoxide of an alkaline earth metal , etc.
  • specific examples thereof include magnesium hydroxide, calcium hydroxide, strontium hydroxide, barium hydroxide, magnesium hydrogen carbonate, calcium hydrogen carbonate, strontium hydrogen carbonate, barium hydrogen carbonate, magnesium carbonate, calcium carbonate, strontium carbonate, barium carbonate, magnesium acetate, calcium acetate, strontium acetate, barium acetate, magnesium stearate, calcium stearate, calcium benzoate and magnesium phenyl phosphate.
  • nitrogen-containing compound examples include quaternary ammonium hydroxides and salts thereof, and amines. Specific examples thereof include: quaternary ammonium hydroxides having e.g. an alkyl group, or an aryl group such as tetramethylammonium hydroxide, tetraethylammonium hydroxide, tetrapropylammonium hydroxide, tetrabutylammonium hydroxide and trimethylbenzylammonium hydroxide; tertiary amines such as triethylamine, dimethylbenzylamine and triphenylamine; secondary amines such as diethylamine and dibutylamine; primary amines such as propylamine and butylamine; imidazoles such as 2-methylimidazole, 2-phenylimidazole and benzimidazole; and bases or basic salts such as ammonia, tetramethylammonium borohydride, tetrabutyl
  • salts of zinc, tin, zirconium, lead, etc. are preferably used. These substances may be used solely, or two or more of them may be used in combination.
  • the transesterification catalyst e.g. zinc acetate, zinc benzoate, zinc 2-ethylhexanoate, tin(II) chloride, tin(IV) chloride, tin(II) acetate, tin(IV) acetate, dibutyltin dilaurate, dibutyltin oxide, dibutyltin dimethoxide, zirconium acetylacetonato, zirconium oxyacetate, zirconium tetrabutoxide, lead(II) acetate, or lead(IV) acetate is specifically used.
  • These catalysts are used at a ratio of 1 ⁇ 10 -9 to 1 ⁇ 10 -3 mol, and preferably 1 ⁇ 10 -7 to 1 ⁇ 10 -4 mol relative to 1 mol of the total of the dihydroxy compounds.
  • the catalyst two or more types of such catalysts may be used in combination. Further, the catalyst itself may be added directly, or may be dissolved in a solvent such as water and phenol and then added.
  • melt polycondensation is carried out while removing a by-product by means of the transesterification reaction under heating conditions and under ordinary pressure or reduced pressure.
  • the catalyst may be present from the start of the reaction together with the raw materials, or may be added in the middle of the reaction.
  • the reaction may be performed with a monohydroxy compound by-produced being retained, but not distilled away.
  • the reaction time is 20 minutes to 240 minutes, preferably 40 minutes to 180 minutes, and particularly preferably 60 minutes to 150 minutes.
  • the monohydroxy compound by-produced is distilled away immediately after it is produced, the content of a high-molecular-weight body in the polycarbonate resin finally obtained is decreased.
  • Preferred reaction time may vary depending on a reaction scale.
  • the melt polycondensation reaction may be either a continuous type or a batch type.
  • the reaction apparatus to be used for performing the reaction may be a vertical apparatus equipped with e.g. an anchor type stirring blade, maxblend stirring blade, helicalribbon type stirring blade, or a horizontal apparatus equipped with e.g. a paddle blade, lattice blade, or spectacle-shaped blade, or an extruder-type apparatus equipped with a screw. Further, use of these reaction apparatuses in combination is suitably carried out in consideration of the viscosity of a polymerized product.
  • the catalyst may be removed or deactivated, but is not necessarily required to be deactivated.
  • a method for deactivating a catalyst by means of addition of a publicly-known acidic substance can be suitably carried out.
  • esters such as butyl benzoate; aromatic sulfonic acids such as p-toluenesulfonic acid; aromatic sulfonic acid esters such as butyl p-toluenesulfonate and hexyl p-toluenesulfonate; phosphoric acids such as phosphorous acid, phosphoric acid and phosphonic acid; phosphorous acid esters such as triphenyl phosphite, monophenyl phosphite, diphenyl phosphite, diethyl phosphite, di-n-propyl phosphite, di-n-butyl phosphite, di-n-hexyl phosphite, dioctyl phosphite and monooctyl phosphite; phosphoric acid esters such as triphenyl phosphate, diphenyl phosphate,
  • deactivating agents are preferably used. From the viewpoint of effects of a deactivating agent, stability against the resin, etc., p-toluene or butyl sulfonate is particularly preferred.
  • These deactivating agents are used in an amount of 0.01 to 50 times, and preferably 0.3 to 20 times the molar quantity of the catalyst. When the amount is less than 0.01 times the molar quantity of the catalyst, the deactivating effect is insufficient and therefore it is undesirable. When the amount is more than 50 times the molar quantity of the catalyst, heat resistance of the resin is reduced and a molded body tends to be easily colored, and therefore it is undesirable.
  • the addition of the deactivating agent can be carried out by means of kneading, and either a continuous type or a batch type may be employed.
  • the temperature at the time of kneading is preferably 200 to 350°C, more preferably 230 to 300°C, and particularly preferably 250 to 270°C.
  • an extruder is suitably used in the case of the continuous type method, and Labo Plastomill or a kneader is suitably used in the case of the batch type method.
  • the extruder include a single screw extruder, a twin screw extruder, a multi-screw extruder, etc.
  • the atmosphere pressure for melting and kneading the resin composition is not particularly limited, and ordinary pressure or reduced pressure, for example, a pressure ranging from ordinary pressure (760 mmHg) to 0.1 mmHg is preferred in terms of antioxidation and removal of decomposed materials and low boiling point components such as phenol.
  • the extruder may be either a vent-type extruder or a non-vent-type extruder, but from the viewpoint of quality improvement of extruded products, preferred is a vent-type extruder.
  • vent pressure may be either ordinary pressure or reduced pressure, but for example, it may be a pressure ranging from ordinary pressure (760 mmHg) to 0.1 mmHg, and it is preferably a pressure of about 100 to 0.1 mmHg, and more preferably a pressure of about 50 to 0.1 mmHg in terms of antioxidation and removal of decomposed materials and low boiling point components such as phenol. Further, hydrogenation and devolatilization may also be carried out for the purpose of more efficiently reducing low boiling point components such as phenol.
  • Kneading of the deactivating agent may be carried out immediately after the polymerization reaction is completed, or may be carried out after the resin after the polymerization is pelletized. Further, in addition to the deactivating agent, other additives (antioxidant, mold release agent, ultraviolet absorber, flowability improving agent, crystal nucleating agent, toughening agent, dye, antistatic agent, antimicrobial agent, etc.) may also be added in a similar manner.
  • additives antioxidant, mold release agent, ultraviolet absorber, flowability improving agent, crystal nucleating agent, toughening agent, dye, antistatic agent, antimicrobial agent, etc.
  • a process of devolatilizing and removing a low boiling point compound in the polymer under a pressure of 0.1 to 1 mmHg and at a temperature of 200 to 350°C may be carried out.
  • the temperature at the time of devolatilizing and removing is preferably 230 to 300°C, and more preferably 250 to 270°C.
  • a horizontal apparatus equipped with a stirring blade having excellent surface renewal ability such as a paddle blade, a lattice blade and a spectacle-shaped blade, or a thin film evaporator is suitably used.
  • the content of foreign materials in the polycarbonate resin is as small as possible, and filtration of a melting raw material, filtration of a catalyst solution, etc. are suitably carried out.
  • the mesh of the filter is preferably 5 ⁇ m or less, and more preferably 1 ⁇ m or less.
  • filtration of the produced resin using a polymer filter is suitably carried out.
  • the mesh of the polymer filter is preferably 100 ⁇ m or less, and more preferably 30 ⁇ m or less.
  • the process of obtaining a resin pellet should definitely be carried out in a low-dust environment, which is preferably Class 6 or lower, and more preferably Class 5 or lower.
  • An optical molded body can be produced using the above-described polycarbonate resin. It is molded according to any method, for example, the injection molding method, compression molding method, extrusion molding method, or solution casting method.
  • the polycarbonate resin used in the present invention is excellent in moldability and heat resistance, and therefore can be advantageously used particularly for optical lenses which require injection molding.
  • the polycarbonate resin used in the present invention can be mixed with another resin such as another polycarbonate resin and a polyester resin to be used.
  • additives such as an antioxidant, a processing stabilizer, a light stabilizer, a heavy metal deactivator, a flame retardant, a lubricant, an antistatic agent, a surfactant, an antimicrobial agent, a mold release agent, an ultraviolet absorber, a plasticizer and a compatibilizer may be mixed therewith.
  • antioxidants examples include triethylene glycol-bis [3 -(3 -tert-butyl-5 -methyl-4-hydroxyphenyl)propionate], 1,6-hexanediol-bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate], pentaerythritol tetrakis [3 -(3,5 -di-tert-butyl-4-hydroxyphenyl)propionate], octadecyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, 1,3,5-trimethyl-2,4,6-tris(3,5-di-tert-butyl-4-hydroxybenzyl)benzene, N,N-hexamethylene bis(3,5-di-tert-butyl-4-hydroxy-hydrocinnamide), 3,5 -di-tert-butyl-4-hydroxy-benzylphosphonate-diethy
  • processing stabilizer examples include a phosphorus-based processing heat stabilizer and a sulfur-based processing heat stabilizer.
  • phosphorus-based processing heat stabilizer examples include phosphorous acid, phosphoric acid, phosphonous acid, phosphonic acid and esters thereof.
  • triphenyl phosphite tris(nonylphenyl) phosphite, tris(2,4-di-tert-butylphenyl) phosphite, tris(2,6-di-tert-butylphenyl) phosphite, tridecyl phosphite, trioctyl phosphite, trioctadecyl phosphite, didecylmonophenyl phosphite, dioctylmonophenyl phosphite, diisopropylmonophenyl phosphite, monobutyldiphenyl phosphite, monodecyldiphenyl phosphite, monooctyldiphenyl phosphite, bis(2,6-di-tert-butyl-4-methylphenyl) pentaerythritol
  • sulfur-based processing heat stabilizer examples include pentaerythritol-tetrakis(3 -lauryl thiopropionate), pentaerythritol-tetrakis(3 -myristyl thiopropionate), pentaerythritol-tetrakis(3-stearyl thiopropionate), dilauryl-3,3 '-thiodipropionate, dimyristyl-3,3 '-thiodipropionate and distearyl-3,3'-thiodipropionate.
  • the content of the sulfur-based processing heat stabilizer in the polycarbonate resin is preferably 0.001 to 0.2 parts by weight relative to 100 parts by weight of the polycarbonate resin.
  • the mold release agent it is preferred that 90 wt% or more of it is made of an ester of an alcohol and a fatty acid.
  • the ester of an alcohol and a fatty acid include an ester of a monohydric alcohol and a fatty acid and a partial ester or whole ester of a polyhydric alcohol and a fatty acid.
  • an ester of a monohydric alcohol and a fatty acid an ester of a monohydric alcohol having 1 to 20 carbon atoms and a saturated fatty acid having 10 to 30 carbon atoms is preferred.
  • partial ester or whole ester of a polyhydric alcohol and a fatty acid a partial ester or whole ester of a polyhydric alcohol having 1 to 25 carbon atoms and a saturated fatty acid having 10 to 30 carbon atoms is preferred.
  • ester of a monohydric alcohol and a saturated fatty acid examples include stearyl stearate, palmityl palmitate, butyl stearate, methyl laurate and isopropyl palmitate.
  • Specific examples of the partial ester or whole ester of a polyhydric alcohol and a saturated fatty acid include whole esters or partial esters of monoglyceride stearate, diglyceride stearate, triglyceride stearate, monosorbitate stearate, monoglyceride behenate, monoglyceride caprate, monoglyceride laurate, pentaerythritol monostearate, pentaerythritol tetrastearate, pentaerythritol tetrapelargonate, propylene glycol monostearate, biphenyl biphenate, sorbitan monostearate, 2-ethylhexyl stearate and dipentaerythritol
  • monoglyceride stearate and monoglyceride laurate are particularly preferred.
  • the content of these mold release agents is preferably 0.005 to 2.0 parts by weight, more preferably 0.01 to 0.6 parts by weight, and even more preferably 0.02 to 0.5 parts by weight relative to 100 parts by weight of the polycarbonate resin.
  • the ultraviolet absorber is preferably at least one ultraviolet absorber selected from the group consisting of a benzotriazole-based ultraviolet absorber, a benzophenone-based ultraviolet absorber, a triazine-based ultraviolet absorber, a cyclic iminoester-based ultraviolet absorber and a cyanoacrylate-based ultraviolet absorber. That is, ultraviolet absorbers mentioned below may be used solely, or two or more of them may be used in combination.
  • benzotriazole-based ultraviolet absorber examples include 2-(2-hydroxy-5-methylphenyl)benzotriazole, 2-(2-hydroxy-5-tert-octylphenyl)benzotriazole, 2-(2-hydroxy-3,5-dicumylphenyl)phenylbenzotriazole, 2-(2-hydroxy-3-tert-butyl-5-methylphenyl)-5-chlorobenzotriazole, 2,2'-methylenebis[4-(1,1,3,3-tetramethylbutyl)-6-(2N-benzotriazol-2-yl)phenol], 2-(2-hydroxy-3,5-di-tert-butylphenyl)benzotriazole, 2-(2-hydroxy-3,5-di-tert-butylphenyl)-5-chlorobenzotriazole, 2-(2-hydroxy-3,5-di-tert-amylphenyl)benzotriazole, 2-(2-hydroxy-5-tert-octylphenyl
  • benzophenone-based ultraviolet absorber examples include 2,4-dihydroxybenzophenone, 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-octoxybenzophenone, 2-hydroxy-4-benzyloxybenzophenone, 2-hydroxy-4-methoxy-5-sulfoxybenzophenone, 2-hydroxy-4-methoxy-5 -sulfoxytrihydrate benzophenone, 2,2' -dihydroxy-4-methoxybenzophenone, 2,2',4,4' -tetrahydroxybenzophenone, 2,2' -dihydroxy-4,4' -dimethoxybenzophenone, 2,2' -dihydroxy-4,4' -dimethoxy-5-sodiumsulfoxybenzophenone, bis(5-benzoyl-4-hydroxy-2-methoxyphenyl)methane, 2-hydroxy-4-n-dodecyloxybenzophonone and 2-hydroxy-4-methoxy-2' -carboxybenzophenone.
  • triazine-based ultraviolet absorber examples include 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-[(hexyl)oxy]-phenol, 2-(4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl)-5-[(octyl)oxy]-phenol and 2,4,6-tris(2-hydroxy-4-hexyloxy-3-methylphenyl)-1,3,5-triazine.
  • Examples of the cyclic iminoester-based ultraviolet absorber include 2,2'-bis(3,1-benzoxazin-4-one), 2,2'-p-phenylenebis(3,1-benzoxazin-4-one), 2,2'-m-phenylenebis(3,1-benzoxazin-4-one), 2,2' -(4,4' -diphenylene)bis(3,1 -benzoxazin-4-one), 2,2'-(2,6-naphthalene)bis(3,1-benzoxazin-4-one), 2,2'-(1,5-naphthalene)bis(3,1-benzoxazin-4-one), 2,2'-(2-methyl-p-phenylene)bis(3,1-benzoxazin-4-one), 2,2'-(2-nitro-p-phenylene)bis(3,1-benzoxazin-4-one) and 2,2'-(2-chloro-p-phenylene)bis(3,1-benzoxazin-4-one
  • cyanoacrylate-based ultraviolet absorber examples include 1,3-bis-[(2'-cyano-3',3'-diphenylacryloyl)oxy]-2,2-bis[(2-cyano-3,3-diphenylacryloyl) oxy]methyl)propane and 1,3-bis-[(2-cyano-3,3-diphenylacryloyl)oxy]benzene.
  • the content of the ultraviolet absorber is preferably 0.01 to 3.0 parts by weight, more preferably 0.02 to 1.0 parts by weight, and even more preferably 0.05 to 0.8 parts by weight relative to 100 parts by weight of the polycarbonate resin. When the content is within these ranges, sufficient weatherability can be imparted to the polycarbonate resin according to intended use.
  • the polycarbonate resin used in the present invention exhibits a high refractive index and excellent heat resistance, and further has flowability appropriate for molding. Moreover, the polycarbonate resin exhibits low birefringence and optical distortion is not easily caused thereby, and therefore, other than as optical lenses, the polycarbonate resin can be advantageously used as a structural material of optical components such as a transparent conductive substrate to be used for a liquid crystal display, an organic EL display, a solar cell, etc., an optical disk, a liquid crystal panel, an optical card, a sheet, a film, an optical fiber, a connector, a vapor-deposited plastic reflection mirror and a display, or as an optical molded body appropriate for use as a functional material.
  • optical components such as a transparent conductive substrate to be used for a liquid crystal display, an organic EL display, a solar cell, etc., an optical disk, a liquid crystal panel, an optical card, a sheet, a film, an optical fiber, a connector, a vapor-deposited plastic reflection mirror and
  • a coat layer such as an antireflection layer, or a hard coat layer may be provided according to need.
  • the antireflection layer may be either a single layer or a multilayer, and may be made of either an organic substance or an inorganic substance, but is preferably made of an inorganic substance. Specific examples thereof include oxides and fluorides such as silicon oxide, aluminium oxide, zirconium oxide, titanium oxide, cerium oxide, magnesium oxide and magnesium fluoride.
  • An optical lens produced by using the polycarbonate resin used in the present invention has a high refractive index and excellent heat resistance, and therefore can be used in the field in which expensive glass lenses having a high refractive index have been conventionally used including telescopes, binoculars and television projectors and is very useful.
  • the optical lens is preferably used in the form of an aspherical lens according to need.
  • the aspherical lens since the spherical aberration can be adjusted to be substantially zero by one lens, it is not necessary to remove the spherical aberration by combining a plurality of spherical lenses, and reduction in weight and reduction in the production cost can be carried out. Accordingly, the aspherical lens is particularly useful as a camera lens among optical lenses.
  • the optical lens is molded by any method such as the injection molding method, the compression molding method and the injection compression molding method.
  • any method such as the injection molding method, the compression molding method and the injection compression molding method.
  • the molding environment In order to avoid mixing of a foreign material in the optical lens as much as possible, the molding environment must be a low-dust environment, and it is preferably Class 6 or lower, and more preferably Class 5 or lower.
  • An optical film produced by using the polycarbonate resin used in the present invention has excellent transparency and heat resistance, and therefore is suitably used for a film for liquid crystal substrates, an optical memory card, etc.
  • the molding environment In order to avoid mixing of a foreign material in the optical film as much as possible, the molding environment must be a low-dust environment, and it is preferably Class 6 or lower, and more preferably Class 5 or lower.
  • the above-described polycarbonate resin may be in the form of a resin composition containing a plurality of resins.
  • the polycarbonate resin composition comprises: a polycarbonate resin (E) having a structural unit (A) derived from a compound represented by general formula (1); and a polycarbonate resin (F) having a structural unit (B) derived from a compound represented by general formula (2) (excluding dicarboxylic acid).
  • the polycarbonate resin composition comprises at least a polycarbonate resin (E) having a structural unit (A) derived from a compound represented by general formula (1) and a polycarbonate resin (F) having a structural unit (B) derived from a compound represented by general formula (2).
  • the polycarbonate resin composition comprises a structural unit derived from preferably a compound represented by general formula (2a) or (2b), and more preferably a compound represented by general formula (2a), which are included in the compound represented by general formula (2).
  • the polycarbonate resin composition may contain another resin in addition to the polycarbonate resin (E) and the polycarbonate resin (F) within a range in which the features of the present invention are not impaired.
  • polycarbonate resin composition examples include: polyethylene, polypropylene, polyvinyl chloride, polystyrene, (meth)acrylic resin, ABS resin, polyamide, polyacetal, polycarbonate (other than the polycarbonate resin (E) and the polycarbonate resin (F)), polyphenylene ether, polyester, polyphenylene sulfide, polyimide, polyether sulfone, polyether ether ketone, fluororesin, cycloolefin polymer, ethylene-vinyl acetate copolymer, epoxy resin, silicone resin, phenol resin, unsaturated polyester resin and polyurethane.
  • the content of the above-described another resin which may be contained in the polycarbonate resin composition is preferably 20 parts by mass or less, and more preferably 10 parts by mass or less relative to the total mass of the polycarbonate resin (E) and the polycarbonate resin (F).
  • the polycarbonate resin (E) is preferably composed of the carbonate unit induced from the structural unit (A), and the polycarbonate resin (F) is preferably composed of the carbonate unit induced from the structural unit (B). Further, a resin composition composed of only the polycarbonate resin (E) and the polycarbonate resin (F) is particularly preferred.
  • the polycarbonate resin composition phenol produced at the time of the production of respective resins constituting the composition and carbonic acid diester which is unreacted and remains are present as impurities.
  • the phenol content in the polycarbonate resin composition is preferably 0.1 to 3000 ppm, more preferably 0.1 to 2000 ppm, and particularly preferably 1 to 1000 ppm, 1 to 800 ppm, 1 to 500 ppm or 1 to 300 ppm.
  • the carbonic acid diester content in the polycarbonate resin composition is preferably 0.1 to 1000 ppm, more preferably 0.1 to 500 ppm, and particularly preferably 1 to 100 ppm.
  • a resin composition having physical properties appropriate for purposes can be obtained.
  • the adjustment of the phenol content and the carbonic acid diester content can be suitably carried out by changing conditions for polycondensation and apparatuses.
  • the adjustment can also be carried out by changing conditions for the extrusion process after polycondensation.
  • the content of phenol or carbonic acid diester When the content of phenol or carbonic acid diester is more than the above-described ranges, it may cause problems such as reduction in the strength of a resin molded body obtained and generation of odor. Meanwhile, when the content of phenol or carbonic acid diester is less than the above-described ranges, it may cause reduction in the plasticity of a resin at the time of melting.
  • the polycarbonate resin (E) comprises the structural unit derived from the compound represented by general formula (1).
  • a repeating structural unit of the polycarbonate resin (E) a structural unit derived from a compound other than the compound represented by general formula (1) may be contained, but the amount thereof is desirably 20 mol% or less, and more desirably 10 mol% or less relative to 100 mol% of the structural unit (A). When the amount is within the above-described ranges, a high refractive index can be retained.
  • the polystyrene equivalent average molecular weight (Mw) of the polycarbonate resin (E) is preferably 20000 to 200000, more preferably 25000 to 120000, and particularly preferably 25000 to 50000.
  • Mw is less than 20000
  • a resin becomes fragile and therefore it is undesirable.
  • Mw is more than 200000
  • the melt viscosity increases, resulting in difficulty in taking out a resin from a mold at the time of molding, and in addition, the flowability is reduced, resulting in difficulty in handling in a molten state, and therefore it is undesirable.
  • the method for producing the polycarbonate resin (E) is not particularly limited.
  • it can be produced by the melt polycondensation method using a dihydroxy compound represented by general formula (1) in the presence of a carbonic acid diester and a catalyst.
  • a catalyst a basic compound catalyst or a transesterification catalyst or a mixed catalyst made of both of them can be used.
  • the polycarbonate resin (E) may contain a structural unit derived from another dihydroxy compound other than the dihydroxy compound represented by general formula (1).
  • another dihydroxy compound include: an aliphatic dihydroxy compound such as ethylene glycol, 1,3-propanediol, 1,2-propanediol, 1,4-butanediol, 1,3-butanediol, 1,2-butanediol, 1,5-heptanediol and 1,6-hexanediol; an alicyclic dihydroxy compound such as 1,2-cyclohexanedimethanol, 1,3-cyclohexanedimethanol, 1,4-cyclohexanedimethanol, tricyclodecanedimethanol, pentacyclopentadecanedimethanol, 2,6-decalindimethanol, 1,5-decalindimethanol, 2,3-decalindimethanol, 2,3-norbornanedimethanol, 2,5-norbornane
  • the above-described another dihydroxy compound is added in an amount of desirably 20 mol% or less, and more desirably 10 mol% or less relative to 100 mol% of the structural unit derived from the dihydroxy compound represented by general formula (1).
  • the amount is within the above-described ranges, a high refractive index can be retained.
  • the method for producing the polycarbonate resin (F) is the same as the above-described method for producing the polycarbonate resin (E), except that the compound represented by general formula (1) is changed to the compound represented by general formula (2).
  • the method for producing the polycarbonate resin composition is not particularly limited.
  • it can be produced by any of the following methods:
  • the polycarbonate resin (E) and the polycarbonate resin (F) are blended together with a weight ratio ((100 ⁇ (E))/((E)+(F))) of preferably 1 to 99%, more preferably 10 to 90%, even more preferably 25 to 60%, and particularly preferably 40 to 70%.
  • the polycarbonate resin composition may contain two or more types of each of the polycarbonate resin (E) and the polycarbonate resin (F).
  • (E) and (F) in the formula (100 ⁇ (E))/((E)+(F)) respectively mean the total weight of the two or more types of the polycarbonate resin (E) and the total weight of the two or more types of the polycarbonate resin (F).
  • the difference of the polystyrene equivalent weight-average molecular weight ( ⁇ Mw) between the polycarbonate resin (E) and the polycarbonate resin (F) is preferably 0 to 120,000, more preferably 0 to 80,000, and particularly preferably 0 to 20,000.
  • ⁇ Mw polystyrene equivalent weight-average molecular weight
  • an antioxidant e.g. an antioxidant, a mold release agent, an ultraviolet absorber, a flowability improving agent, a toughening agent, a crystal nucleating agent, a dye, an antistatic agent, or an antimicrobial agent may be added according to need.
  • additives may be added in advance to each or either of the polycarbonate resin (E) and the polycarbonate resin (F) before performing kneading, and may be added and kneaded simultaneously at the time of kneading or may be kneaded after mixing.
  • the polycarbonate resin composition may contain a polycarbonate resin other than the polycarbonate resin (E) and the polycarbonate resin (F), but more preferably, does not substantially contain such a polycarbonate resin.
  • antioxidant processing stabilizer, mold release agent and ultraviolet absorber contained in the resin composition
  • the same things as those described in "(3) Optical molded body obtained by using polycarbonate resin" above can be used, and the same adding amounts can also be employed.
  • an optical molded body such as an optical lens and an optical film can be produced according to methods similar to those described in "(3) Optical molded body obtained by using polycarbonate resin" above.
  • the polycarbonate resin composition of the embodiment is excellent in moldability and heat resistance, and therefore can be advantageously used particularly for optical lenses which require injection molding.
  • Preferred physical properties of the polycarbonate resin composition and the molded body are as described below.
  • the molecular weight (polystyrene equivalent weight-average molecular weight (Mw)) of the polycarbonate resin composition of the embodiment (after mixing) is preferably 20000 to 200000, more preferably 25000 to 120000, and particularly preferably 25000 to 50000.
  • the glass transition temperature of the polycarbonate resin composition of the embodiment is preferably 95°C to 180°C, and more preferably 115°C to 160°C.
  • the refractive index of the molded body produced from the polycarbonate resin composition of the embodiment is preferably 1.640 to 1.680, and more preferably 1.650 to 1.670.
  • the Abbe number of the molded body produced from the polycarbonate resin composition of the embodiment is preferably 24 or less, and more preferably 23 or less.
  • optical distortion of the polycarbonate resin composition of the embodiment when a molded piece of the polycarbonate resin composition is sandwiched between two polarizing plates and light leakage from behind is visually observed according to the crossed-Nicol method, it is preferred that light leakage is not significant, but is slight.
  • the molded body produced from the polycarbonate resin composition of the embodiment exhibits low birefringence, it is suitable for a structural material of optical components such as a lens, an optical film and an optical sheet. It is particularly suitable for optical components such as a lens because it has high transparency as well as low birefringence.
  • a coat layer such as an antireflection layer, or a hard coat layer may be provided according to need.
  • the antireflection layer may be either a single layer or a multilayer, and may be made of either an organic substance or an inorganic substance, but is preferably made of an inorganic substance. Specific examples thereof include oxides and fluorides such as silicon oxide, aluminium oxide, zirconium oxide, titanium oxide, cerium oxide, magnesium oxide and magnesium fluoride.
  • the polyester resin of the embodiment has a structural unit derived from a dihydroxy compound represented by general formula (1) (hereinafter sometimes referred to as “structural unit (G)”) and a structural unit derived from a dihydroxy compound represented by general formula (2) (hereinafter sometimes referred to as “structural unit (H)").
  • structural unit (G) a structural unit derived from a dihydroxy compound represented by general formula (1)
  • structural unit (H) a structural unit derived from a dihydroxy compound represented by general formula (2)
  • the structural units are bound to each other via an ester bond.
  • the ester bond is also referred to as "structural unit derived from a dicarboxylic acid or a derivative thereof' or “dicarboxylic acid structural unit”.
  • X represents a C 1-10 alkylene group.
  • a compound represented by general formula (2a) and a compound represented by general formula (2b) can be suitably used.
  • R 1 and R 2 are as defined with respect to formula (2) above.
  • R 1 and R 2 are as defined with respect to formula (2) above.
  • structural unit (I) the structural unit derived from the compound represented by general formula (2a) is sometimes referred to as "structural unit (I)".
  • the ratio of the total of the dihydroxy structural unit and the dicarboxylic acid structural unit in all the structural units of the polyester resin is preferably 80 mol% or more, more preferably 90 mol% or more, and particularly preferably 100 mol%.
  • the polyester resin of the embodiment may contain a structural unit derived from a dihydroxy compound other than the structural units (G) to (I), and examples of the dihydroxy compound (excluding dicarboxylic acid and derivatives thereof) include alkylene glycols (e.g, linear or branched C 2-12 alkylene glycols such as ethylene glycol, propylene glycol, trimethylene glycol, 1,3-butanediol, tetramethylene glycol (1,4-butanediol), hexanediol, neopentylglycol, octanediol and decanediol), and (poly)oxyalkylene glycols (e.g., diethylene glycol, triethylene glycol, dipropylene glycol).
  • alkylene glycols e.g, linear or branched C 2-12 alkylene glycols such as ethylene glycol, propylene glycol, trimethylene glycol, 1,3-butaned
  • one type may be contained solely, or two or more types may be contained in combination.
  • the ratio of the structural unit derived from ethylene glycol in all the dihydroxy structural units is preferably 5 to 70 mol%, and more preferably 5 to 40 mol%.
  • the ratio of the structural unit (G) in all the dihydroxy structural units (excluding the structural unit derived from dicarboxylic acid) is preferably 5 to 95 mol%, and more preferably 60 to 95%.
  • the content of the structural unit (H) is preferably 95 to 5 mol%, and more preferably 40 to 5 mol% relative to all the dihydroxy structural units (excluding the structural unit derived from dicarboxylic acid). The same applies to the case where the structural unit (H) is the structural unit (I).
  • the molar ratio between the structural unit (G) and the structural unit (H) (G/H) is preferably 40/60 to 99/1, more preferably 60/40 to 95/5, and particularly preferably 70/30 to 90/10.
  • the dicarboxylic acid structural unit contained in the polyester resin of the embodiment is not particularly limited, but preferred are structural units derived from: aromatic dicarboxylic acids such as naphthalene dicarboxylic acid, terephthalic acid, isophthalic acid, phthalic acid, 2-methylterephthalic acid, biphenyl dicarboxylic acid and tetralin dicarboxylic acid; aliphatic dicarboxylic acids such as oxalic acid, malonic acid, succinic acid, maleic acid, fumaric acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, decanedicarboxylic acid, dodecanedicarboxylic acid, cyclohexanedicarboxylic acid, decalin dicarboxylic acid, norbornane dicarboxylic acid, tricyclodecanedicarboxylic acid, pentacyclododecanedicarbox
  • Examples of derivatives of these dicarboxylic acids include esters, acid anhydrides and acid halides.
  • structural units derived from a dicarboxylic acid represented by general formula (3) and a derivative thereof are also preferred.
  • Ys each independently represent a single bond, a C 1-20 alkyl group, a C 1-20 alkoxyl group, a C 5-20 cycloalkyl group, a C 5-20 cycloalkoxyl group, a C 6-20 aryl group or a C 6-20 aryloxy group.
  • the dicarboxylic acid structural unit constituting the polyester resin of the embodiment may be composed of one of the structural units mentioned above, or two or more of the structural units.
  • the polyester resin may have a structure of either a random copolymer, block copolymer or alternating copolymer.
  • the above-described polyester resin can be produced by reacting a compound by which the dicarboxylic acid structural unit is produced (e.g., dicarboxylic acids, and esters, acid anhydrides and acid halides thereof) with a compound by which the dihydroxy structural unit is produced (e.g., dihydroxy compounds, excluding structural units derived from dicarboxylic acids).
  • a compound by which the dicarboxylic acid structural unit is produced e.g., dicarboxylic acids, and esters, acid anhydrides and acid halides thereof
  • a compound by which the dihydroxy structural unit is produced e.g., dihydroxy compounds, excluding structural units derived from dicarboxylic acids.
  • reaction method examples include various methods such as the melt polymerization method including the transesterification method and the direct polymerization method, the solution polymerization method and the interfacial polymerization method. Among them, the melt polymerization method not using a reaction solvent is preferred.
  • the dicarboxylic acid or a derivative thereof is preferably used at a ratio of 0.90 to 1.01 mol relative to 1 mol of the total of the dihydroxy compounds.
  • the transesterification method that is one of melt polymerization methods is a method of obtaining a polyester by reacting a dicarboxylic acid ester with the dihydroxy compound (excluding the dicarboxylic acid) in the presence of a catalyst and performing transesterification while distilling away an alcohol produced, and it is generally used for synthesis of a polyester resin.
  • the direct polymerization method is a method of obtaining a polyester resin by performing a dehydration reaction of the dicarboxylic acid and the dihydroxy compound (excluding the dicarboxylic acid) to form an ester compound and then performing a transesterification reaction while distilling away an excess of the dihydroxy compound under reduced pressure.
  • the direct polymerization method has the advantages that distillation of an alcohol is not performed unlike the transesterification method and that an inexpensive dicarboxylic acid can be used as a raw material.
  • the type of the polymerization catalyst the amount of the catalyst, polymerization conditions such as temperature, and additives such as a heat stabilizer, an etherification prevention agent and a catalyst deactivator for performing these melt polymerization methods, publicly-known methods can be referred to.
  • the reaction may be performed in the presence of a catalyst.
  • a metal catalyst for example, various catalysts to be utilized for the production of polyester resins, for example, a metal catalyst can be used.
  • a metal catalyst for example, a metal compound including an alkali metal, an alkaline earth metal, a transition metal, a metal belonging to Group 13 of the periodic table, a metal belonging to Group 14 of the periodic table, or a metal belonging to Group 15 of the periodic table is used.
  • the metal compound include alkoxides, organic acid salts (acetates, propionates, etc.), inorganic acid salts (borates, carbonates, etc.) and metal oxides. These catalysts may be used solely, or two or more of them may be used in combination.
  • the amount of the catalyst to be used may be, for example, about 0.01 ⁇ 10 -4 to 100 ⁇ 10 -4 mol, and preferably about 0.1 ⁇ 10 -4 to 40 ⁇ 10 -4 mol relative to 1 mol of the dicarboxylic acid.
  • alkali metal compound examples include sodium hydroxide, potassium hydroxide, cesium hydroxide, lithium hydroxide, sodium hydrogen carbonate, sodium carbonate, potassium carbonate, cesium carbonate, lithium carbonate, sodium acetate, potassium acetate, cesium acetate, lithium acetate, sodium stearate, potassium stearate, cesium stearate, stearium, potassium benzoate, cesium benzoate, lithium benzoate, disodium hydrogen phosphate, dipotassium hydrogen phosphate, dilithium hydrogen phosphate, disodium phenyl phosphate, a disodium salt, dipotassium salt, dicesium salt or dilithium salt of bisphenol A, and a sodium salt, potassium salt, cesium salt or lithium salt of phenol.
  • alkaline earth metal compound examples include magnesium hydroxide, calcium hydroxide, strontium hydroxide, barium hydroxide, magnesium hydrogen carbonate, calcium hydrogen carbonate, strontium hydrogen carbonate, barium hydrogen carbonate, magnesium carbonate, calcium carbonate, strontium carbonate, barium carbonate, magnesium acetate, calcium acetate, strontium acetate, barium acetate, magnesium stearate, calcium stearate, calcium benzoate and magnesium phenyl phosphate.
  • salts of zinc, tin, zirconium and lead are preferably used. These substances may be used solely, or two or more of them may be used in combination.
  • These catalysts are used at a ratio of generally about 1 ⁇ 10 -9 to 1 ⁇ 10 -3 mol, and preferably about 1 ⁇ 10 -7 to 1 ⁇ 10 -4 mol relative to 1 mol of the total of the dihydroxy compounds (excluding the dicarboxylic acid).
  • various additives such as an antioxidant, a mold release agent, a light stabilizer, an ultraviolet absorber, a plasticizer, an extender, a matting agent, a drying regulator, an antistatic agent, an anti-settling agent, a surfactant, a flowability improving agent, a drying oil, a wax, a filler, a coloring agent, a reinforcing agent, a surface smoothing agent, a leveling agent, a curing reaction accelerator and a thickener, and a molding aid can be added.
  • additives such as an antioxidant, a mold release agent, a light stabilizer, an ultraviolet absorber, a plasticizer, an extender, a matting agent, a drying regulator, an antistatic agent, an anti-settling agent, a surfactant, a flowability improving agent, a drying oil, a wax, a filler, a coloring agent, a reinforcing agent, a surface smoothing agent, a leveling agent, a curing reaction accelerator and a thickener,
  • an ester of a multifunctional alcohol and a fatty acid, particularly a stearic acid ester of glycerin is preferably added in an amount of 0.005 to 2.0 parts by weight, preferably 0.01 to 0.6 parts by weight, and more preferably 0.02 to 0.5 parts by weight relative to 100 parts by weight of the polyester resin, thereby reducing troubles due to mold release failure.
  • the catalyst in order not to impair thermal stability and hydrolytic stability of the obtained polyester resin, it is preferred to remove or deactivate the catalyst after the polymerization reaction is completed.
  • the catalyst can be deactivated by means of addition of a publicly-known acidic substance.
  • aromatic sulfonic acids such as p-toluenesulfonic acid; aromatic sulfonic acid esters such as butyl p-toluenesulfonate and hexyl p-toluenesulfonate; aromatic sulfonates such as dodecylbenzenesulfonic acid tetrabutylphosphonium salt; organic halides such as stearic acid chloride, benzoyl chloride and p-toluenesulfonic acid chloride; alkyl sulfates such as dimethyl sulfate; organic halides such as benzyl chloride; etc. are preferably used.
  • the content of foreign materials in the polyester resin of the embodiment is as small as possible, and filtration of a melting raw material, filtration of a catalyst solution and filtration of a melting oligomer are preferably carried out.
  • the mesh of the filter is preferably 7 ⁇ m or less, and more preferably 5 ⁇ m or less.
  • filtration of the produced resin using a polymer filter is preferably carried out.
  • the mesh of the polymer filter is preferably 100 ⁇ m or less, and more preferably 30 ⁇ m or less.
  • the process of obtaining a resin pellet should definitely be carried out in a low-dust environment, which is preferably Class 6 or lower, and more preferably Class 5 or lower.
  • the refractive index and the Abbe number can be measured according to the below-described methods.
  • the polyester resin is dissolved in methylene chloride to produce a cast film, and the refractive index is measured by a refractometer.
  • the value of the refractive index is measured at 25°C and at 589 nm (d line), and the value of the Abbe number is calculated from refractive indexes measured at 656 nm (C line), 486 nm (F line) and d line.
  • the refractive index measured in this way is preferably 1.60 or more, and more preferably 1.645 to 1.70. Further, the Abbe number is preferably 21 or less, more preferably 20 or less, and for example, 17 to 21.
  • the glass transition temperature is measured by a differential scanning calorimeter and is not particularly limited, but is usually 110°C or higher, preferably 115°C or higher, and more preferably 120°C or higher.
  • an optical lens produced by using the resin is sufficiently resistant to the surface treatment including hard coating.
  • glass transition temperatures of the polyester resin and the polyester carbonate resin can be easily set to be 110°C or higher by suitably selecting a conventionally-known diol or dicarboxylic acid (e.g., a diol having a cyclic acetal skeleton or aromatic hydrocarbon group, a dicarboxylic acid having a naphthalene skeleton).
  • the glass transition temperature is preferably lower than 150°C.
  • the above-described polyester resin can be used for various applications.
  • it can be used for an injection molded body, a sheet, a film, an extrusion molded body such as a pipe, a bottle, a foam, an adhesive material, an adhesive and a paint.
  • the sheet may be either a single layer or a multilayer
  • the film may also be either a single layer or a multilayer and may be unstretched or stretched in one direction or two directions, and may be laminated e.g. on a steel plate.
  • the bottle may be either a direct blow bottle or an injection blow bottle, and may be obtained by injection molding.
  • the foam may be either a bead foam or an extruded foam.
  • the polyester resin can be particularly preferably used for applications requiring high heat resistance and water vapor barrier properties, for example, products used in automobiles, packaging materials for import and export, electronic materials such as back sheets of solar cells, and food packaging materials for retorting or heating with a microwave oven.
  • the molding environment must be a low-dust environment, and it is preferably Class 6 or lower, and more preferably Class 5 or lower.
  • the optical lens obtained by molding the polyester resin is preferably used in the form of an aspherical lens according to need.
  • the aspherical lens since the spherical aberration can be adjusted to be substantially zero by one lens, it is not necessary to remove the spherical aberration by combining a plurality of spherical lenses, and reduction in weight and reduction in the production cost can be carried out. Accordingly, the aspherical lens is particularly useful as a camera lens among optical lenses.
  • the astigmatism of the aspherical lens is preferably 0 to 15 m ⁇ , and more preferably 0 to 10 m ⁇ .
  • a coat layer such as an antireflection layer, or a hard coat layer may be provided according to need.
  • the antireflection layer may be either a single layer or a multilayer, and may be made of either an organic substance or an inorganic substance, but is preferably made of an inorganic substance. Specific examples thereof include oxides and fluorides such as silicon oxide, aluminium oxide, zirconium oxide, titanium oxide, cerium oxide, magnesium oxide and magnesium fluoride.
  • the optical lens obtained by molding the polyester resin can be used as various lenses such as a pickup lens, an f- ⁇ lens and a spectacle lens, but because of its high refractive index and low Abbe number, it can be particularly preferably used as a lens for correction of chromatic aberration.
  • the optical lens is preferably used as a lens of a single-lens reflex camera, a digital still camera, a video camera, a cellular phone with e.g. a camera, a disposable camera, a telescope, binoculars, a microscope, or a projector.
  • the optical lens obtained by using the polyester resin of the embodiment is a concave lens, it can be combined with another convex lens having a high Abbe number to be used as an optical lens system having a small chromatic aberration.
  • the Abbe number of the convex lens to be combined is preferably 40 to 60, and more preferably 50 to 60.
  • the polyester carbonate resin of the embodiment has a structural unit (L) derived from a dihydroxy compound represented by general formula (1) and a structural unit (M) derived from a dihydroxy compound represented by general formula (2).
  • the structural units are bound to each other via a carbonate bond and an ester bond.
  • the carbonate bond is also referred to as "structural unit derived from a carbonic acid diester", and the ester bond is also referred to as "structural unit derived from a dicarboxylic acid or a derivative thereof' or “dicarboxylic acid structural unit”.
  • X represents a C 1-10 alkylene group.
  • a compound represented by general formula (2a) and a compound represented by general formula (2b) can be suitably used.
  • R 1 and R 2 are as defined with respect to formula (2) above.
  • R 1 and R 2 are as defined with respect to formula (2) above.
  • structural unit (N) the structural unit derived from the compound represented by general formula (2a) is sometimes referred to as "structural unit (N)".
  • the ratio of the total of the dihydroxy structural unit (excluding the structural unit derived from dicarboxylic acid), the carbonic acid diester structural unit and the dicarboxylic acid structural unit in all the structural units of the polyester carbonate resin is preferably 80 mol% or more, more preferably 90 mol% or more, and particularly preferably 100 mol%.
  • the ratio of the structural unit (L) in all the dihydroxy structural units (excluding the dicarboxylic acid structural unit) is preferably 5 to 95 mol%.
  • the content of the structural unit (M) is preferably 2.5 to 47.5 mol%, and more preferably 5 to 45 mol% relative to all the dihydroxy structural units (including the dicarboxylic acid structural unit). The same applies to the case where the structural unit (M) is the structural unit (N).
  • the molar ratio between the structural unit (L) and the structural unit (M) (L/M) is preferably 1/99 to 99/1, more preferably 20/80 to 95/5, and particularly preferably 40/60 to 90/10.
  • the polyester carbonate resin may have a structure of either a random copolymer, block copolymer or alternating copolymer.
  • the polyester carbonate resin of the embodiment may contain a structural unit derived from a dihydroxy compound other than the structural units (L) to (N), and examples of the dihydroxy compound (excluding dicarboxylic acid and derivatives thereof) include alkylene glycols (e.g, linear or branched C 2-12 alkylene glycols such as ethylene glycol, propylene glycol, trimethylene glycol, 1,3-butanediol, tetramethylene glycol (1,4-butanediol), hexanediol, neopentylglycol, octanediol and decanediol), and (poly)oxyalkylene glycols (e.g., diethylene glycol, triethylene glycol, dipropylene glycol).
  • alkylene glycols e.g, linear or branched C 2-12 alkylene glycols such as ethylene glycol, propylene glycol, trimethylene glycol, 1,3-butan
  • one type may be contained solely, or two or more types may be contained in combination.
  • Examples of the carbonic acid diester which is a precursor of a carbonate bond include diphenyl carbonate, ditolyl carbonate, bis(chlorophenyl) carbonate, m-cresyl carbonate, dimethyl carbonate, diethyl carbonate, dibutyl carbonate and dicyclohexyl carbonate.
  • diphenyl carbonate is particularly preferred.
  • Diphenyl carbonate is used at a ratio of preferably 0.97 to 1.10 mol, and more preferably 0.98 to 1.05 mol relative to 1 mol of the total of the dihydroxy compounds.
  • the structural unit derived from the dicarboxylic acid contained in the polyester carbonate resin of the embodiment is not particularly limited, but preferred are structural units derived from: aromatic dicarboxylic acids such as naphthalene dicarboxylic acid, terephthalic acid, isophthalic acid, phthalic acid, 2-methylterephthalic acid, biphenyl dicarboxylic acid and tetralin dicarboxylic acid; aliphatic dicarboxylic acids such as oxalic acid, malonic acid, succinic acid, maleic acid, fumaric acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, decanedicarboxylic acid, dodecanedicarboxylic acid, cyclohexanedicarboxylic acid, decalin dicarboxylic acid, norbornane dicarboxylic acid, tricyclodecanedicarboxylic acid, pentacyclodo
  • Examples of derivatives of these dicarboxylic acids include esters, acid anhydrides and acid halides.
  • structural units derived from a dicarboxylic acid represented by general formula (3) and a derivative thereof are also preferred.
  • Ys each independently represent a single bond, a C 1-20 alkyl group, a C 1-20 alkoxyl group, a C 5-20 cycloalkyl group, a C 5-20 cycloalkoxyl group, a C 6-20 aryl group or a C 6-20 aryloxy group.
  • the dicarboxylic acid structural unit may be composed of one of the structural units mentioned above, or two or more of the structural units.
  • the above-described polyester carbonate resin can be produced by performing a transesterification reaction of a compound by which the carbonic acid diester structural unit is produced, a compound by which the dicarboxylic acid structural unit is produced and a compound by which the dihydroxy structural unit is produced in a molten state in the presence of the catalyst.
  • the compound represented by general formula (1), the compound represented by general formula (2) (preferably the compound represented by general formula (2a) or (2b)), a dicarboxylic acid or a derivative thereof, and a carbonic acid diester are reacted.
  • the reaction method include various methods such as the melt polymerization method including the transesterification method and the direct polymerization method, the solution polymerization method and the interfacial polymerization method. Among them, the melt polymerization method not using a reaction solvent is preferred.
  • the carbonic acid diester is used at a ratio of preferably 0.97 to 1.10 mol, and more preferably 0.98 to 1.05 mol relative to 1 mol of the total of the dihydroxy compounds. Further, the dicarboxylic acid or a derivative thereof is used at a ratio of preferably 0.01 to 0.20 mol, and more preferably 0.05 to 0.15 mol relative to 1 mol of the total of the dihydroxy compounds (excluding the dicarboxylic acid).
  • the transesterification method that is one of melt polymerization methods is a method of obtaining a polyester by reacting a dicarboxylic acid ester with the dihydroxy compound (excluding the dicarboxylic acid) in the presence of a catalyst and performing transesterification while distilling away an alcohol produced, and it is generally used for synthesis of a polyester resin.
  • the direct polymerization method is a method of obtaining a polyester resin by performing a dehydration reaction of the dicarboxylic acid and the dihydroxy compound (excluding the dicarboxylic acid) to form an ester compound and then performing a transesterification reaction while distilling away an excess of the dihydroxy compound under reduced pressure.
  • the direct polymerization method has the advantages that distillation of an alcohol is not performed unlike the transesterification method and that an inexpensive dicarboxylic acid can be used as a raw material.
  • the type of the polymerization catalyst the amount of the catalyst, polymerization conditions such as temperature, and additives such as a heat stabilizer, an etherification prevention agent and a catalyst deactivator for performing these melt polymerization methods, publicly-known methods can be referred to.
  • the reaction may be performed in the presence of a catalyst.
  • a metal catalyst for example, various catalysts to be utilized for the production of polyester carbonate resins, for example, a metal catalyst can be used.
  • a metal catalyst for example, a metal compound including an alkali metal, an alkaline earth metal, a transition metal, a metal belonging to Group 13 of the periodic table, a metal belonging to Group 14 of the periodic table, or a metal belonging to Group 15 of the periodic table is used.
  • the metal compound include alkoxides, organic acid salts (acetates, propionates, etc.), inorganic acid salts (borates, carbonates, etc.) and metal oxides. These catalysts may be used solely, or two or more of them may be used in combination.
  • the amount of the catalyst to be used may be, for example, about 0.01 ⁇ 10 -4 to 100 ⁇ 10 -4 mol, and preferably about 0.1 ⁇ 10 -4 to 40 ⁇ 10 -4 mol relative to 1 mol of the dicarboxylic acid
  • alkali metal compound examples include sodium hydroxide, potassium hydroxide, cesium hydroxide, lithium hydroxide, sodium hydrogen carbonate, sodium carbonate, potassium carbonate, cesium carbonate, lithium carbonate, sodium acetate, potassium acetate, cesium acetate, lithium acetate, sodium stearate, potassium stearate, cesium stearate, stearium, potassium benzoate, cesium benzoate, lithium benzoate, disodium hydrogen phosphate, dipotassium hydrogen phosphate, dilithium hydrogen phosphate, disodium phenyl phosphate, a disodium salt, dipotassium salt, dicesium salt or dilithium salt of bisphenol A, and a sodium salt, potassium salt, cesium salt or lithium salt of phenol.
  • alkaline earth metal compound examples include magnesium hydroxide, calcium hydroxide, strontium hydroxide, barium hydroxide, magnesium hydrogen carbonate, calcium hydrogen carbonate, strontium hydrogen carbonate, barium hydrogen carbonate, magnesium carbonate, calcium carbonate, strontium carbonate, barium carbonate, magnesium acetate, calcium acetate, strontium acetate, barium acetate, magnesium stearate, calcium stearate, calcium benzoate and magnesium phenyl phosphate.
  • salts of zinc, tin, zirconium and lead are preferably used. These substances may be used solely, or two or more of them may be used in combination.
  • These catalysts are used at a ratio of generally 1 ⁇ 10 -9 to 1 ⁇ 10 -3 mol, and preferably 10 -7 to 10 -4 mol relative to 1 mol of the total of the dihydroxy compounds (excluding the dicarboxylic acid).
  • polyester carbonate resin To the polyester carbonate resin, other resins, various additives such as an antioxidant, a mold release agent, a light stabilizer, an ultraviolet absorber, a plasticizer, an extender, a matting agent, a drying regulator, an antistatic agent, an anti-settling agent, a surfactant, a flowability improving agent, a drying oil, a wax, a filler, a coloring agent, a reinforcing agent, a surface smoothing agent, a leveling agent, a curing reaction accelerator and a thickener, and a molding aid can be added. Specific examples, adding amounts, etc. of these additives are as described in "1. Polycarbonate resin" above.
  • an ester of a multifunctional alcohol and a fatty acid, particularly a stearic acid ester of glycerin is preferably added in an amount of 0.005 to 2.0 parts by weight, preferably 0.01 to 0.6 parts by weight, and more preferably 0.02 to 0.5 parts by weight relative to 100 parts by weight of the polyester carbonate resin, thereby reducing troubles due to mold release failure.
  • the catalyst in order not to impair thermal stability and hydrolytic stability of the obtained polyester carbonate resin, it is preferred to remove or deactivate the catalyst after the polymerization reaction is completed.
  • the catalyst can be deactivated by means of addition of a publicly-known acidic substance.
  • aromatic sulfonic acids such as p-toluenesulfonic acid; aromatic sulfonic acid esters such as butyl p-toluenesulfonate and hexyl p-toluenesulfonate; aromatic sulfonates such as dodecylbenzenesulfonic acid tetrabutylphosphonium salt; organic halides such as stearic acid chloride, benzoyl chloride and p-toluenesulfonic acid chloride; alkyl sulfates such as dimethyl sulfate; organic halides such as benzyl chloride; etc. are preferably used.
  • the content of foreign materials in the polyester carbonate resin of the embodiment is as small as possible, and filtration of a melting raw material, filtration of a catalyst solution and filtration of a melting oligomer are preferably carried out.
  • the mesh of the filter is preferably 7 ⁇ m or less, and more preferably 5 ⁇ m or less.
  • filtration of the produced resin using a polymer filter is preferably carried out.
  • the mesh of the polymer filter is preferably 100 ⁇ m or less, and more preferably 30 ⁇ m or less.
  • the process of obtaining a resin pellet should definitely be carried out in a low-dust environment, which is preferably Class 6 or lower, and more preferably Class 5 or lower.
  • the refractive index and the Abbe number can be measured according to the below-described measurement methods.
  • the polyester carbonate resin is dissolved in methylene chloride to produce a cast film, and the refractive index is measured by a refractometer.
  • the value of the refractive index is measured at 25°C and at 589 nm (d line), and the value of the Abbe number is calculated from refractive indexes measured at 656 nm (C line), 486 nm (F line) and d line.
  • the refractive index measured in this way is preferably 1.60 or more, and more preferably 1.645 to 1.665. Further, the Abbe number is preferably 24 or less, more preferably 21 or less, and for example, 18 to 24.
  • the glass transition temperature is measured by a differential scanning calorimeter and is not particularly limited, but is usually 110°C or higher, preferably 115°C or higher, and more preferably 120°C or higher.
  • an optical lens produced by using the resin is sufficiently resistant to the surface treatment including hard coating.
  • glass transition temperatures of the polyester resin and the polyester carbonate resin can be easily set to be 110°C or higher by suitably selecting a conventionally-known diol or dicarboxylic acid (e.g., a diol having a cyclic acetal skeleton or aromatic hydrocarbon group, a dicarboxylic acid having a naphthalene skeleton).
  • the glass transition temperature is preferably lower than 150°C.
  • the polystyrene equivalent weight-average molecular weight (Mw) is preferably 10000 to 100000, and more preferably 20000 to 50000.
  • Mw is less than 10000
  • a resin molded body obtained tends to be fragile and therefore it is undesirable.
  • Mw is more than 100000, the melt viscosity increases, resulting in difficulty in taking out a resin from a mold at the time of molding, and in addition, the flowability is reduced, resulting in difficulty in injection molding in a molten state, and therefore it is undesirable.
  • the color phase of the solution (brightness; L value) is measured according to the method shown in the Examples, and is preferably 88 or more, and more preferably 95 to 99.
  • L value is less than 88, the resin is more strongly colored, resulting in difficulty in use thereof as an optical material, and therefore it is undesirable.
  • polyester carbonate resin of the embodiment The limiting viscosity and the semicrystallization time of the polyester carbonate resin of the embodiment are the same as those described in "2. Polyester resin" above.
  • the resin of the embodiment preferably satisfies the below-described physical properties (1) and (2) simultaneously.
  • the above-described polyester carbonate resin can be used for various applications.
  • it can be used for an injection molded body, a sheet, a film, an extrusion molded body such as a pipe, a bottle, a foam, an adhesive material, an adhesive and a paint.
  • the sheet may be either a single layer or a multilayer
  • the film may also be either a single layer or a multilayer and may be unstretched or stretched in one direction or two directions, and may be laminated on e.g. a steel plate.
  • the bottle may be either a direct blow bottle or an injection blow bottle, and may be obtained by injection molding.
  • the foam may be either a bead foam or an extruded foam.
  • the polyester resin can be particularly preferably used for applications requiring high heat resistance and water vapor barrier properties, for example, products used in automobiles, packaging materials for import and export, electronic materials such as back sheets of solar cells, and food packaging materials for retorting or heating with a microwave oven.
  • the molding environment must be a low-dust environment, and it is preferably Class 6 or lower, and more preferably Class 5 or lower.
  • the optical lens obtained by molding the polyester carbonate resin is preferably used in the form of an aspherical lens according to need.
  • the aspherical lens since the spherical aberration can be adjusted to be substantially zero by one lens, it is not necessary to remove the spherical aberration by combining a plurality of spherical lenses, and reduction in weight and reduction in the production cost can be carried out. Accordingly, the aspherical lens is particularly useful as a camera lens among optical lenses.
  • the astigmatism of the aspherical lens is preferably 0 to 15 m ⁇ , and more preferably 0 to 10 m ⁇ .
  • a hard coat layer may be provided according to need.
  • the antireflection layer may be either a single layer or a multilayer, and may be made of either an organic substance or an inorganic substance, but is preferably made of an inorganic substance. Specific examples thereof include oxides and fluorides such as silicon oxide, aluminium oxide, zirconium oxide, titanium oxide, cerium oxide, magnesium oxide and magnesium fluoride.
  • the optical lens obtained by molding the polyester carbonate resin can be used as various lenses such as a pickup lens, an f- ⁇ lens and a spectacle lens, but because of its high refractive index and low Abbe number, it can be particularly preferably used as a lens for correction of chromatic aberration.
  • the optical lens is preferably used as a lens of e.g. a single-lens reflex camera, a digital still camera, a video camera, a cellular phone with a camera, a disposable camera, a telescope, binoculars, a microscope, or a projector.
  • the optical lens obtained by using the polyester carbonate resin of the embodiment is a concave lens, it can be combined with another convex lens having a high Abbe number to be used as an optical lens system having a small chromatic aberration.
  • the Abbe number of the convex lens to be combined is preferably 40 to 60, and more preferably 50 to 60.
  • BHEBN 2,2'-bis(2-hydroxyethoxy)-1,1'-binaphthalene
  • BPEF 9,9-bis(4-(2-hydroxyethoxy)phenyl)fluorene
  • DPC diphenyl carbonate
  • 8.8 ⁇ 10 -5 g 1.0 ⁇ 10 6 mol of sodium hydrogen carbonate
  • the temperature was increased to 240°C at a rate of 60°C/hr, and a reaction was performed with stirring for 30 minutes. After the reaction was completed, nitrogen was blown into the reactor to adjust the pressure to ordinary pressure, and a polycarbonate resin produced was taken out therefrom.
  • the amount of residual phenol was 150 ppm
  • the amount of residual DPC was 120 ppm.
  • Example 2 The operation was carried out in a manner similar to that in Example 1, except that the amounts of BHEBN, BPEF, DPC and sodium hydrogen carbonate were changed to 17.1 g (0.046 mol), 30.1 g (0.069 mol), 25.0 g (0.117 mol) and 8.7 ⁇ 10 -5 g (1.0 ⁇ 10 6 mol), respectively, and a polycarbonate resin produced was taken out.
  • the amount of residual phenol was 60 ppm
  • the amount of residual DPC was 250 ppm.
  • Example 2 The operation was carried out in a manner similar to that in Example 1, except that the amounts of BHEBN, BPEF, DPC and sodium hydrogen carbonate were changed to 30.0 g (0.080 mol), 15.1 g (0.034 mol), 25.0 g (0.117 mol) and 8.7 ⁇ 10 -5 g (1.0 ⁇ 10 6 mol), respectively, and a polycarbonate resin produced was taken out.
  • the amount of residual phenol was 120 ppm.
  • Example 2 The operation was carried out in a manner similar to that in Example 1, except that the amounts of BHEBN, BPEF, DPC and sodium hydrogen carbonate were changed to 38.9 g (0.104 mol), 5.07 g (0.012 mol), 25.0 g (0.117 mol) and 1.1 ⁇ 10 -4 g (1.3 ⁇ 10 -6 mol), respectively, and a polycarbonate resin produced was taken out.
  • the amount of residual phenol was 100 ppm.
  • Example 2 The operation was carried out in a manner similar to that in Example 1, except that the time of stirring performed under the same conditions after heating to 180°C under nitrogen atmosphere (760 mmHg) and confirming complete dissolution of the raw materials was reduced from 110 minutes to 30 minutes and that the final pressure reducing degree was adjusted to 50 mmHg, and a polycarbonate resin produced was taken out.
  • the amount of residual phenol was 3500 ppm
  • the amount of residual DPC was 1200 ppm.
  • BPA bisphenol A
  • Each of the polycarbonate resins obtained in Examples 1-4, Reference Example 1 and Comparative Example 1 was dissolved in methylene chloride to prepare a resin solution in which the solid component concentration was 5.3 wt%.
  • This resin solution was poured into a mold for the production of a cast film, and released and dried after volatilization of methylene chloride, thereby preparing a cast film having a thickness of 0.1 mm.
  • the refractive index (nD), the Abbe number (v) and the total light transmittance of the cast film were evaluated. Further, the obtained cast film was stretched 1.5-fold at a temperature of Tg + 5°C to evaluate the orientation birefringence ( ⁇ n).
  • BHEBN 2,2'-bis(2-hydroxyethoxy)-1,1'-binaphthalene
  • BEPF 9,9-bis(4-(2-hydroxyethoxy)-3-phenylphenyl)fluorene
  • DPC diphenyl carbonate
  • 1.5 ⁇ 10 -4 g (1.8 ⁇ 10 -6 mol) of sodium hydrogen carbonate were put into a 300 ml four-neck flask equipped with a stirrer and a distillation apparatus, and it was heated to 180°C under nitrogen atmosphere (760 mmHg).
  • Example 7 The operation was carried out in a manner similar to that in Example 7, except that the amounts of BHEBN, BEPF, DPC and sodium hydrogen carbonate were changed to 5.17 g (0.014 mol), 19.0 g (0.032 mol), 10.0 g (0.047 mol) and 9.7 ⁇ 10 -5 g (1.2 ⁇ 10 -6 mol), respectively, and a polycarbonate resin produced was taken out.
  • Example 7 The operation was carried out in a manner similar to that in Example 7, except that the amounts of BHEBN, BEPF, DPC and sodium hydrogen carbonate were changed to 13.8 g (0.037 mol), 32.6 g (0.055 mol), 20.0 g (0.093 mol) and 1.5 ⁇ 10 -4 g (1.8 ⁇ 10 -6 mol), respectively, and a polycarbonate resin produced was taken out.
  • Example 7 The operation was carried out in a manner similar to that in Example 7, except that the amounts of BHEBN, BEPF, DPC and sodium hydrogen carbonate were changed to 24.4 g (0.065 mol), 16.5 g (0.028 mol), 20.2 g (0.094 mol) and 1.6 ⁇ 10 -4 g (1.9 ⁇ 10 -6 mol), respectively, and a polycarbonate resin produced was taken out.
  • Example 7 The operation was carried out in a manner similar to that in Example 7, except that the amounts of BHEBN, BEPF, DPC and sodium hydrogen carbonate were changed to 31.0 g (0.083 mol), 5.4 g (0.009 mol), 20.0 g (0.093 mol) and 1.5 ⁇ 10 -4 g (1.8 ⁇ 10 -6 mol), respectively, and a polycarbonate resin produced was taken out.
  • BPA bisphenol A
  • the start of distillation of by-produced phenol was confirmed. After that, the temperature was kept for 20 minutes to perform a reaction. Further, the temperature was increased to 230°C at a rate of 75°C/hr, and 10 minutes after the end of the increase of the temperature, the temperature was kept while the pressure reducing degree was adjusted to 1 mmHg or less over 1 hour. After that, the temperature was increased to 240°C at a rate of 60°C/hr, and a reaction was performed with stirring for 30 minutes. After the reaction was completed, nitrogen was blown into the reactor to adjust the pressure to ordinary pressure, and a polycarbonate resin produced was taken out therefrom.
  • Each of the polycarbonate resins obtained in Examples 7-11, Comparative Example 2 and Reference Example 2 was dissolved in methylene chloride to prepare a resin solution in which the solid component concentration was 5.3 wt%.
  • This resin solution was poured into a mold for the production of a cast film, and released and dried after volatilization of methylene chloride, thereby preparing a cast film having a thickness of 0.1 mm.
  • the refractive index (nD), the Abbe number (v) and the total light transmittance of the cast film were evaluated. Further, the obtained cast film was stretched 1.5-fold at a temperature of Tg + 5°C to evaluate the orientation birefringence ( ⁇ n).
  • the temperature was increased to 230°C at a rate of 45°C/hr, and conditions were kept at 230°C and 200 mmHg for 10 minutes.
  • the pressure reducing degree was adjusted to 150 mmHg over 20 minutes, and conditions were kept at 230°C and 150 mmHg for 10 minutes.
  • the pressure reducing degree was adjusted to 120 mmHg over 10 minutes, and conditions were kept at 230°C and 120 mmHg for 70 minutes.
  • the pressure reducing degree was adjusted to 100 mmHg over 10 minutes, and conditions were kept at 230°C and 100 mmHg for 10 minutes.
  • the pressure reducing degree was adjusted to 1 mmHg or less over 40 minutes, and stirring was performed under conditions of 230°C and 1 mmHg or less for 30 minutes to perform a polymerization reaction. After the reaction was completed, nitrogen was blown into the reactor to increase the pressure, and a polycarbonate resin produced was taken out therefrom while being pelletized.
  • Mw was 33000
  • Tg was 115°C
  • residual phenol was 300 ppm
  • residual DPC was 250 ppm.
  • the temperature was increased to 240°C at a rate of 37.5°C/hr, and conditions were kept at 240°C and 150 mmHg for 10 minutes.
  • the pressure reducing degree was adjusted to 120 mmHg over 10 minutes, and conditions were kept at 240°C and 120 mmHg for 70 minutes.
  • the pressure reducing degree was adjusted to 100 mmHg over 10 minutes, and conditions were kept at 240°C and 100 mmHg for 10 minutes.
  • the pressure reducing degree was adjusted to 1 mmHg or less over 40 minutes, and stirring was performed under conditions of 240°C and 1 mmHg or less for 10 minutes to perform a polymerization reaction.
  • a pellet of a polycarbonate resin made of bisphenol A type polycarbonate resin "Iupilon H-4000" (trade name, manufactured by Mitsubishi Engineering-Plastics Corporation, Mw: 33000) was injection-molded to obtain a circular plate having a diameter of 50 mm and a thickness of 3 mm. The circular plate was transparent.
  • the evaluation results are shown in Table 7.
  • the pellet produced in Synthesis Example 1 was injection-molded to obtain a circular plate having a diameter of 50 mm and a thickness of 3 mm.
  • the circular plate was transparent.
  • the evaluation results are shown in Table 7.
  • DMT dimethyl terephthalate
  • BPEF 9,9-bis[4-(2-hydroxyethoxy)phenyl]fluorene
  • BHEBN 2,2'-bis(2-hydroxyethoxy)-1,1'-binaphthalene
  • the mixture was gradually heated and melted with stirring under nitrogen atmosphere in the presence of zinc acetate dihydrate in an amount of 0.023 mol% relative to the dicarboxylic acid component to perform an esterification reaction.
  • germanium oxide in an amount of 0.14 mol%
  • triethyl phosphate in an amount of 0.12 mol% relative to 100 mol% of the dicarboxylic acid component were added.
  • the temperature was gradually increased and the pressure was gradually reduced, ethylene glycol was removed while reducing the pressure, and finally, polycondensation was performed at 250 to 280°C and 0.1 kPa or less. After that, the content was taken out from the reactor, and a copolymerized polyester resin having a fluorene skeleton was obtained.
  • the polystyrene equivalent weight-average molecular weight of the obtained polyester resin was 42,000. Evaluation of physical properties is shown in Table 8.
  • Example 8 The operation was carried out in a manner similar to that in Example 1, except that the amounts of BPEF and BHEBN were changed to 0.27 mol and 0.63 mol, respectively, and that DMT was changed to dimethyl 2,6-naphthalenedicarboxylate (hereinafter abbreviated as "NDCM"). As a result, a polyester copolymer having a weight average molecular weight of 40,500 was obtained. Evaluation of physical properties is shown in Table 8.
  • a transesterification reaction and a polycondensation reaction were performed using the same apparatus and reaction conditions as those in Example 18 above, except that the raw materials and feed amounts were changed to those described in Table 8, and a copolymerized polyester resin was obtained.
  • the results of evaluation of physical properties of the obtained resin are shown in Table 8.
  • BHEBN 2,2'-bis(2-hydroxyethoxy)-1,1'-binaphthalene
  • BPEF 9,9-bis(4-(2-hydroxyethoxy)phenyl)fluorene
  • DPC diphenyl carbonate
  • DMT dimethyl terephthalate
  • the rotational speed was increased to 200 rpm, the pressure was reduced to 200 mmHg at a rate of 28 mmHg/min, and the temperature was increased to 260°C at a rate of 60°C/hr. During this, the start of distillation of by-produced phenol was confirmed. After the pressure reached 200 mmHg and the temperature reached 260°C, the pressure was reduced at 10 mmHg/min. After the pressure reached 0.8 mmHg, the reaction was completed. Nitrogen was blown into the reactor to adjust the pressure to ordinary pressure, and a polyester carbonate resin produced was taken out therefrom.

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Claims (19)

  1. Résine de polyester, comprenant :
    un motif structurel dérivé d'un composé représenté par la formule générale (1) ci-dessous :
    Figure imgb0059
     dans laquelle X représente un groupe alkylène en C1 à C10 ;
    un motif structurel dérivé d'un composé représenté par la formule générale (2) ci-dessous :
    Figure imgb0060
    dans laquelle R1 et R2 représentent chacun indépendamment un atome d'hydrogène, un groupe alkyle en C1 à C20, un groupe alcoxyle en C1 à C20, un groupe cycloalkyle en C5 à C20, un groupe cycloalcoxyle en C5 à C20, un groupe aryle en C6 à C20, ou un groupe aryloxy en C6 à C20 et R représente un atome d'hydrogène ou un groupe hydroxyalkyle en C1 à C20 ; et
    un motif structurel dérivé d'un acide dicarboxylique ou d'un dérivé de celui-ci.
  2. Résine de polyester selon la revendication 1, dans laquelle le composé représenté par la formule générale (2) est un composé représenté par la formule générale (2a) ci-dessous :
    Figure imgb0061
     dans laquelle R1 et R2 sont tels que définis dans la revendication 1,
    ou un composé représenté par la formule générale (2b) ci-dessous :
    Figure imgb0062
     dans laquelle R1 et R2 sont tels que définis dans la revendication 1.
  3. Résine de polyester selon la revendication 1 ou 2, dans laquelle l'acide dicarboxylique ou un dérivé de celui-ci est l'acide naphtalène dicarboxylique, l'acide téréphtalique, l'acide isophtalique, un acide dicarboxylique contenant un groupe fluorène ou un ester de ceux-ci.
  4. Résine de polyester selon l'une quelconque des revendications 1 à 3, dans laquelle dans les motifs structurels dérivés d'un composé dihydroxy dans la résine de polyester, la proportion du motif structurel dérivé du composé représenté par la formule générale (1) est de 5 à 95 % en mole et la proportion du motif structurel dérivé du composé représenté par la formule générale (2) est de 2,5 à 47,5 % en mole.
  5. Résine de polyester selon l'une quelconque des revendications 1 à 4, comprenant en outre un motif structurel dérivé du glycol, dans laquelle dans les motifs structurels dérivés du composé dihydroxy dans la résine de polyester, la proportion du motif structurel dérivé du glycol est de 5 à 70 % en mole.
  6. Élément optique comprenant la résine de polyester selon l'une quelconque des revendications 1 à 5.
  7. Élément optique selon la revendication 6, qui est une lentille optique d'un appareil photo réflexe à un objectif, d'un appareil photographique numérique, d'une caméra vidéo, d'un téléphone cellulaire ayant une caméra, d'un appareil photo jetable, d'un télescope, d'un binoculaire, d'un microscope ou d'un projecteur.
  8. Résine de polyester carbonate, comprenant :
    un motif structurel dérivé d'un composé représenté par la formule générale (1) ci-dessous :
    Figure imgb0063
     dans laquelle X représente un groupe alkylène en C1 à C10 ;
    un motif structurel dérivé d'un composé représenté par la formule générale (2) ci-dessous :
    Figure imgb0064
    dans laquelle R1 et R2 représentent chacun indépendamment un atome d'hydrogène, un groupe alkyle en C1 à C20, un groupe alcoxyle en C1 à C20, un groupe cycloalkyle en C5 à C20, un groupe cycloalcoxyle en C5 à C20, un groupe aryle en C6 à C20 ou un groupe aryloxy en C6 à C20 et R représente un atome d'hydrogène ou un groupe hydroxyalkyle en C1 à C20 ;
    un motif structurel dérivé d'un acide dicarboxylique ou d'un dérivé de celui-ci ; et
    un motif structurel dérivé d'un diester d'acide carbonique.
  9. Résine de polyester carbonate selon la revendication 8, dans laquelle le composé représenté par la formule générale (2) est un composé représenté par la formule générale (2a) ci-dessous :
    Figure imgb0065
     dans laquelle R1 et R2 sont tels que définis dans la revendication 8,
    ou un composé représenté par la formule générale (2b) ci-dessous :
    Figure imgb0066
     dans laquelle R1 et R2 sont tels que définis dans la revendication 8.
  10. Résine de polyester carbonate selon la revendication 8 ou 9, dans laquelle l'acide dicarboxylique ou un dérivé de celui-ci est l'acide naphtalène dicarboxylique, l'acide téréphtalique, l'acide isophtalique, un acide dicarboxylique contenant un groupe fluorène ou un ester de ceux-ci.
  11. Résine de polyester carbonate selon l'une quelconque des revendications 8 à 10, dans laquelle dans les motifs structurels dérivés d'un composé dihydroxy dans la résine de polyester carbonate, la proportion du motif structurel dérivé du composé représenté par la formule générale (1) est de 5 à 95 % en mole et la proportion du motif structurel dérivé du composé représenté par la formule générale (2) est de 2,5 à 47,5 % en mole.
  12. Résine de polyester carbonate selon l'une quelconque des revendications 8 à 11, qui présente un indice de réfraction de 1,645 à 1,660, mesuré selon le procédé de la norme JIS-K-7142 à 23 °C et à une longueur d'onde 589 nm au moyen d'un film présentant une épaisseur de 0,1 mm et d'un réfractomètre d'Abbe.
  13. Résine de polyester carbonate selon l'une quelconque des revendications 8 à 12, qui présente un poids moléculaire moyen en poids (Mw) en équivalent polystyrène de 14 000 à 100 000, mesuré en utilisant une chromatographie par perméation sur gel (GPC) et du tétrahydrofurane comme solvant de développement.
  14. Élément optique comprenant la résine de polyester carbonate selon l'une quelconque des revendications 8 à 13.
  15. Élément optique selon la revendication 14, qui est une lentille optique d'un appareil photo réflexe à un objectif, d'un appareil photographique numérique, d'une caméra vidéo, d'un téléphone cellulaire ayant une caméra, d'un appareil photo jetable, d'un télescope, d'un binoculaire, d'un microscope ou d'un projecteur.
  16. Composition de résine, qui comprend :
    une résine de polycarbonate comprenant :
    un motif structurel dérivé d'un composé représenté par la formule générale (1) ci-dessous :
    Figure imgb0067
     dans laquelle X représente un groupe alkylène en C1 à C10 ;
    un motif structurel dérivé d'un composé représenté par la formule générale (2) ci-dessous :
    Figure imgb0068
     dans laquelle R1 et R2 représentent chacun indépendamment un atome d'hydrogène, un groupe alkyle en C1 à C20, un groupe alcoxyle en C1 à C20, un groupe cycloalkyle en C5 à C20, un groupe cycloalcoxyle en C5 à C20, un groupe aryle en C6 à C20, ou un groupe aryloxy en C6 à C20 et R représente un atome d'hydrogène ou un groupe hydroxyalkyle en C1 à C20 ; et
    un antioxydant ; et/ou
    un agent de démoulage.
  17. Composition de résine selon la revendication 16, dans laquelle l'antioxydant est le tétrakis[3-(3,5-di-tert-butyl-4-hydroxyphényl)propionate] de pentaérythritol.
  18. Composition de résine selon la revendication 16 ou 17, dans laquelle l'agent de démoulage est un ester d'un alcool et d'un acide gras.
  19. Composition de résine selon la revendication 18, dans laquelle l'ester d'un alcool et d'un acide gras est le stéarate de monoglycéride ou le laurate de monoglycéride.
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Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI716369B (zh) * 2014-12-04 2021-01-21 日商三菱瓦斯化學股份有限公司 含有聚酯樹脂之功能性薄片及使用其之透鏡
KR102623133B1 (ko) * 2015-11-04 2024-01-09 미츠비시 가스 가가쿠 가부시키가이샤 수지 조성물의 제조 방법
CN106916288B (zh) * 2015-12-24 2019-08-30 远东新世纪股份有限公司 经改质的共聚酯组成物
WO2017146023A1 (fr) * 2016-02-24 2017-08-31 富士フイルム株式会社 Résine de polycarbonate, corps moulé , composant optique et lentille
JP6680650B2 (ja) * 2016-08-30 2020-04-15 帝人株式会社 ポリエステル樹脂
WO2018181157A1 (fr) * 2017-03-31 2018-10-04 三菱瓦斯化学株式会社 Composition de résine polycarbonate et lentille optique l'utilisant
CN115960345A (zh) * 2017-08-30 2023-04-14 三菱瓦斯化学株式会社 聚碳酸酯树脂、其制造方法和光学透镜
WO2019044214A1 (fr) 2017-08-30 2019-03-07 帝人株式会社 Résine thermoplastique et élément optique
KR102499266B1 (ko) * 2017-10-19 2023-02-13 삼성전자주식회사 디스플레이 장치
CN108131632A (zh) * 2017-12-13 2018-06-08 柏涛涛 一种智能型的太阳能路灯
CN111527125B (zh) * 2017-12-28 2022-07-22 帝人株式会社 聚(酯)碳酸酯和聚(酯)碳酸酯的制造方法
WO2019146507A1 (fr) * 2018-01-23 2019-08-01 三菱瓦斯化学株式会社 Composition de résine de polycarbonate, son procédé de production et lentille optique
TWI823908B (zh) 2018-03-12 2023-12-01 日商帝人股份有限公司 聚酯樹脂或聚酯碳酸酯樹脂及使用該樹脂之光學構件
EP3778699B1 (fr) 2018-03-30 2023-04-12 Teijin Limited Résine de polycarbonate et élément optique la contenant
US11110688B2 (en) * 2018-07-05 2021-09-07 Toray Plastics (America), Inc. Anti-blush and chemical resistant polyester film
US11732088B2 (en) 2018-10-16 2023-08-22 Mitsubishi Gas Chemical Company, Inc. Polyester carbonate resin and optical lens
KR20210080449A (ko) * 2018-10-19 2021-06-30 미츠비시 가스 가가쿠 가부시키가이샤 다환 화합물
KR20210114919A (ko) * 2018-12-27 2021-09-24 미츠비시 가스 가가쿠 가부시키가이샤 수지 조성물, 성형체, 광학 렌즈, 및 광학 렌즈 유닛
WO2021014962A1 (fr) * 2019-07-19 2021-01-28 帝人株式会社 Résine thermoplastique et élément optique la contenant
JP7512757B2 (ja) 2020-08-13 2024-07-09 三菱瓦斯化学株式会社 樹脂組成物並びにそれを含む光学レンズ及び光学フィルム
JP7506173B2 (ja) 2020-10-27 2024-06-25 帝人株式会社 熱可塑性樹脂及びそれを含む光学部材
CN112961336B (zh) * 2021-04-09 2023-01-13 万华化学集团股份有限公司 一种具有稳定高折射率的聚碳酸酯树脂及制备方法和应用
KR20240108368A (ko) * 2021-11-30 2024-07-09 미츠비시 가스 가가쿠 가부시키가이샤 열가소성 수지를 포함하는 광학 렌즈
CN115716912B (zh) * 2022-11-04 2023-09-19 万华化学集团股份有限公司 一种耐黄变热塑性树脂组合物及其制备方法和应用
CN115926135A (zh) * 2022-11-17 2023-04-07 万华化学集团股份有限公司 一种光学形成体用热塑性树脂组合物及其制造方法

Family Cites Families (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5043237A (en) * 1990-01-12 1991-08-27 E. I. Du Pont De Nemours And Company Inhibitor-containing photohardenable electrostatic master compositions having improved resolution
EP0653451B1 (fr) * 1992-07-30 1999-02-17 Kanebo, Ltd. Polyester
IL115803A (en) * 1994-11-03 2000-02-17 Ppg Industries Inc Indeno-naphthopyran derivatives useful for photochromic articles
JP3331121B2 (ja) * 1996-05-17 2002-10-07 カネボウ株式会社 ポリエステル重合体およびその成形体
US5955520A (en) * 1996-06-17 1999-09-21 Ppg Industries, Inc. Photochromic indeno-fused naphthopyrans
US5723072A (en) * 1996-06-17 1998-03-03 Ppg Industries, Inc. Photochromic heterocyclic fused indenonaphthopyrans
JPH1087800A (ja) * 1996-09-10 1998-04-07 Teijin Chem Ltd ポリエステルカーボネート樹脂
CN1234796A (zh) * 1996-10-02 1999-11-10 Ppg工业公司 新的取代萘并吡喃化合物
JP2000302857A (ja) 1999-04-21 2000-10-31 Mitsubishi Gas Chem Co Inc 光記録媒体用成形材料
JP2001072872A (ja) 1999-07-02 2001-03-21 Konica Corp 樹脂組成物および光学用レンズ
JP2002332345A (ja) 2001-05-08 2002-11-22 Konica Corp 樹脂組成物及び光学用レンズ
US6946227B2 (en) * 2002-11-20 2005-09-20 Xerox Corporation Imaging members
JP4281998B2 (ja) * 2003-06-06 2009-06-17 三菱瓦斯化学株式会社 ポリカーボネート樹脂組成物
JP4908781B2 (ja) 2005-06-06 2012-04-04 大阪瓦斯株式会社 ポリエステル樹脂組成物および光学部品
JP2007057916A (ja) * 2005-08-25 2007-03-08 Mitsubishi Gas Chem Co Inc 光学レンズ
JP5005949B2 (ja) * 2006-05-01 2012-08-22 出光興産株式会社 ポリカーボネート系樹脂組成物、光学成形品及び照明ユニット
JP5245824B2 (ja) * 2006-06-05 2013-07-24 三菱瓦斯化学株式会社 光学レンズ
JP2009067681A (ja) * 2007-09-10 2009-04-02 Mitsubishi Chemicals Corp ビスフェニルフルオレンジカルボン酸ジエステルの製造方法、並びにこれを重合してなるポリマー
JP2010100770A (ja) 2008-10-27 2010-05-06 Mitsubishi Gas Chemical Co Inc 熱可塑性樹脂の製造方法、ポリエステル樹脂及びポリカーボネート樹脂、ならびにそれらの用途
JP5526579B2 (ja) 2009-04-06 2014-06-18 三菱瓦斯化学株式会社 ポリカーボネート樹脂組成物、並びにそれを用いた成形品の製造方法及び成形品
JP5617186B2 (ja) 2009-04-20 2014-11-05 三菱瓦斯化学株式会社 ポリカーボネート樹脂組成物
JP5437106B2 (ja) * 2010-02-19 2014-03-12 大阪ガスケミカル株式会社 フルオレン骨格を有するポリエステル樹脂
JP6087490B2 (ja) 2010-10-06 2017-03-01 帝人株式会社 フルオレン誘導体からなる熱可塑性樹脂およびその溶融重合方法
CN103328536A (zh) 2011-01-19 2013-09-25 帝人株式会社 聚酯碳酸酯共聚物及其制造方法
JP5914259B2 (ja) * 2011-08-29 2016-05-11 大阪ガスケミカル株式会社 フルオレン骨格を有するポリエステル樹脂
JP5914261B2 (ja) 2011-08-29 2016-05-11 大阪ガスケミカル株式会社 フルオレン骨格を有するポリエステル樹脂
EP3750939B1 (fr) * 2012-11-07 2023-05-24 Mitsubishi Gas Chemical Company, Inc. Résine de polycarbonate, son procédé de fabrication et corps moulé optique
JP6154337B2 (ja) * 2013-02-20 2017-06-28 帝人株式会社 ポリカーボネート共重合体
JP6139258B2 (ja) * 2013-05-13 2017-05-31 帝人株式会社 ポリエステルカーボネート共重合体

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

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US20220282038A1 (en) 2022-09-08
US20200190259A1 (en) 2020-06-18
CN109593196B (zh) 2021-08-13
TWI662059B (zh) 2019-06-11
CN106255712A (zh) 2016-12-21
CN106255712B (zh) 2018-12-18
US10689486B2 (en) 2020-06-23
KR20170005792A (ko) 2017-01-16
TW201546110A (zh) 2015-12-16
JP6631514B2 (ja) 2020-01-15
CN109593196A (zh) 2019-04-09
US11370882B2 (en) 2022-06-28
JP2020045492A (ja) 2020-03-26
JP6908092B2 (ja) 2021-07-21
EP3483197A1 (fr) 2019-05-15
JPWO2015170691A1 (ja) 2017-04-20
EP3141570A4 (fr) 2018-01-10
US20170044312A1 (en) 2017-02-16
WO2015170691A1 (fr) 2015-11-12
EP3141570A1 (fr) 2017-03-15

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